A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3624396



Internal ID7011252
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:102184034..102205705hg38UCSC Ensembl
Innerchr10:102184034..102205705hg38UCSC Ensembl
Outerchr10:102183534..102206205hg38UCSC Ensembl
chr10:103943791..103965462hg19UCSC Ensembl
Innerchr10:103943791..103965462hg19UCSC Ensembl
Outerchr10:103943291..103965962hg19UCSC Ensembl
Cytoband10q24.32
Allele length
AssemblyAllele length
hg3821672
hg1921672
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv13913680
SamplesNA18749
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3624396
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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