A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3634995



Internal ID7021795
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:76967915..76968996hg38UCSC Ensembl
Innerchr14:76967915..76968996hg38UCSC Ensembl
Outerchr14:76967617..76969272hg38UCSC Ensembl
chr14:77434258..77435339hg19UCSC Ensembl
Innerchr14:77434258..77435339hg19UCSC Ensembl
Outerchr14:77433960..77435615hg19UCSC Ensembl
Cytoband14q24.3
Allele length
AssemblyAllele length
hg381082
hg191082
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15068988, essv15068997, essv15069003, essv15068992, essv15068996, essv15068993, essv15068986, essv15068984, essv15068990, essv15068999, essv15068989, essv15069000, essv15068985, essv15068995, essv15068991, essv15068987, essv15069006, essv15068998, essv15069005, essv15069004, essv15068994, essv15069001, essv15069002
SamplesNA19466, HG03558, HG03193, NA18916, HG02502, HG03714, HG04225, HG03088, NA19327, HG02577, NA19099, HG02675, HG04026, HG02308, NA19324, NA19360, HG03419, HG02974, NA19472, HG02107, NA18876, HG01431, HG03198
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3634995
Frequency
Sample Size2504
Observed Gain0
Observed Loss23
Observed Complex0
Frequencyn/a


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