A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv666334



Internal ID15402986
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:55678647..55968948hg38UCSC Ensembl
Innerchr10:57438407..57728708hg19UCSC Ensembl
Innerchr10:57108413..57398714hg18UCSC Ensembl
Innerchr10:57108413..57398714hg17UCSC Ensembl
Cytoband10q21.1
Allele length
AssemblyAllele length
hg38290302
hg19290302
hg18290302
hg17290302
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv516121
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv666334
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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