A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3622239



Internal ID7009098
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:5872727..5874035hg38UCSC Ensembl
Innerchr10:5872951..5873975hg38UCSC Ensembl
Outerchr10:5872562..5874200hg38UCSC Ensembl
chr10:5914690..5915998hg19UCSC Ensembl
Innerchr10:5914914..5915938hg19UCSC Ensembl
Outerchr10:5914525..5916163hg19UCSC Ensembl
Cytoband10p15.1
Allele length
AssemblyAllele length
hg381309
hg191309
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv13687165, essv13687161, essv13687159, essv13687163, essv13687164, essv13687156, essv13687160, essv13687162, essv13687157, essv13687158, essv13687166
SamplesHG03280, NA19107, HG03199, NA18498, NA06984, HG02642, HG01183, HG02666, HG02839, HG02814, HG02974
Known GenesANKRD16
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3622239
Frequency
Sample Size2504
Observed Gain0
Observed Loss11
Observed Complex0
Frequencyn/a


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