A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3621094



Internal ID7007964
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:93049434..93050369hg38UCSC Ensembl
Innerchr9:93049458..93050346hg38UCSC Ensembl
Outerchr9:93049411..93050393hg38UCSC Ensembl
chr9:95811716..95812651hg19UCSC Ensembl
Innerchr9:95811740..95812628hg19UCSC Ensembl
Outerchr9:95811693..95812675hg19UCSC Ensembl
Cytoband9q22.31
Allele length
AssemblyAllele length
hg38936
hg19936
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv13560020, essv13559978, essv13559977, essv13559992, essv13559989, essv13560021, essv13560029, essv13559997, essv13559971, essv13560034, essv13560015, essv13560030, essv13559990, essv13559980, essv13560002, essv13559968, essv13560014, essv13560026, essv13559996, essv13559970, essv13559976, essv13559973, essv13559985, essv13560022, essv13560035, essv13560017, essv13559981, essv13560005, essv13559987, essv13560011, essv13560006, essv13560007, essv13559991, essv13560018, essv13560010, essv13559974, essv13560031, essv13560036, essv13559979, essv13560019, essv13559994, essv13559986, essv13560025, essv13559982, essv13560001, essv13560033, essv13559998, essv13559984, essv13560023, essv13560009, essv13560000, essv13560016, essv13560013, essv13560037, essv13559983, essv13560003, essv13560012, essv13560028, essv13559995, essv13559972, essv13560027, essv13559993, essv13560008, essv13560032, essv13559969, essv13560024, essv13559988, essv13559975, essv13560004, essv13559999
SamplesNA19394, HG01986, HG03111, NA19378, HG03130, NA18486, HG02870, NA19920, NA19314, NA19379, HG03168, HG02810, HG03105, NA19023, NA19771, NA19384, HG02922, NA19130, HG02981, HG02634, NA19917, NA19372, NA19172, NA19471, NA19317, HG02471, NA20412, HG02946, HG03267, NA19456, HG02715, NA19027, HG02819, HG02716, HG02977, NA19327, HG03027, HG02497, HG03563, NA19114, HG02817, HG03078, NA18856, HG02283, NA19320, NA18853, NA19452, NA19395, NA19625, HG02722, NA19256, NA19149, HG03367, HG01958, HG01272, HG02839, NA19248, HG02974, NA19351, NA19713, HG03351, NA18873, HG02679, NA19711, HG03162, HG01617, NA19430, HG02855, NA19129, HG02343
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3621094
Frequency
Sample Size2504
Observed Gain0
Observed Loss70
Observed Complex0
Frequencyn/a


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