A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3624289



Internal ID6664456
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:95953322..96028771hg38UCSC Ensembl
Innerchr10:95953322..96028771hg38UCSC Ensembl
Outerchr10:95952822..96029271hg38UCSC Ensembl
chr10:97713079..97788528hg19UCSC Ensembl
Innerchr10:97713079..97788528hg19UCSC Ensembl
Outerchr10:97712579..97789028hg19UCSC Ensembl
Cytoband10q24.1
Allele length
AssemblyAllele length
hg3875450
hg1975450
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv13905515
SamplesNA18924
Known GenesCC2D2B, ENTPD1-AS1
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3624289
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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