A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3623905



Internal ID7010761
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:78949442..78949871hg38UCSC Ensembl
Innerchr10:78949447..78949867hg38UCSC Ensembl
Outerchr10:78949438..78949876hg38UCSC Ensembl
chr10:80709199..80709628hg19UCSC Ensembl
Innerchr10:80709204..80709624hg19UCSC Ensembl
Outerchr10:80709195..80709633hg19UCSC Ensembl
Cytoband10q22.3
Allele length
AssemblyAllele length
hg38430
hg19430
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv13867018, essv13867022, essv13867026, essv13867020, essv13867016, essv13867017, essv13867021, essv13867015, essv13867014, essv13867027, essv13867012, essv13867029, essv13867019, essv13867025, essv13867023, essv13867028, essv13867024, essv13867013
SamplesHG01586, HG04211, HG03668, NA20846, HG04042, HG04144, HG01455, HG03696, HG04047, HG03685, HG02789, HG03713, HG03974, NA20870, HG04015, HG03646, HG02681, NA20908
Known GenesZMIZ1-AS1
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3623905
Frequency
Sample Size2504
Observed Gain0
Observed Loss18
Observed Complex0
Frequencyn/a


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