A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv687099



Internal ID15077065
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:8050720..8051222hg38UCSC Ensembl
Innerchr10:8092683..8093185hg19UCSC Ensembl
Innerchr10:8132689..8133191hg18UCSC Ensembl
Innerchr10:8132689..8133191hg17UCSC Ensembl
Cytoband10p14
Allele length
AssemblyAllele length
hg38503
hg19503
hg18503
hg17503
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv517198
Supporting Variants
Samples
Known GenesGATA3-AS1
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv687099
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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