A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3622670



Internal ID7009528
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:25504988..25523267hg38UCSC Ensembl
Innerchr10:25505001..25523254hg38UCSC Ensembl
Outerchr10:25504975..25523280hg38UCSC Ensembl
chr10:25793917..25812196hg19UCSC Ensembl
Innerchr10:25793930..25812183hg19UCSC Ensembl
Outerchr10:25793904..25812209hg19UCSC Ensembl
Cytoband10p12.1
Allele length
AssemblyAllele length
hg3818280
hg1918280
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv13724475, essv13724474
SamplesHG02152, HG00478
Known GenesGPR158
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3622670
Frequency
Sample Size2504
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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