A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3622908



Internal ID7009766
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:35887482..35889150hg38UCSC Ensembl
Innerchr10:35887518..35889115hg38UCSC Ensembl
Outerchr10:35887447..35889186hg38UCSC Ensembl
chr10:36176410..36178078hg19UCSC Ensembl
Innerchr10:36176446..36178043hg19UCSC Ensembl
Outerchr10:36176375..36178114hg19UCSC Ensembl
Cytoband10p11.21
Allele length
AssemblyAllele length
hg381669
hg191669
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv13753907, essv13753906
SamplesHG01500, HG00245
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3622908
Frequency
Sample Size2504
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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