A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv655351



Internal ID15392003
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:11437771..11440050hg38UCSC Ensembl
Innerchr10:11479770..11482049hg19UCSC Ensembl
Innerchr10:11519776..11522055hg18UCSC Ensembl
Innerchr10:11519776..11522055hg17UCSC Ensembl
Cytoband10p14
Allele length
AssemblyAllele length
hg382280
hg192280
hg182280
hg172280
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv515865
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv655351
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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