A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv683555



Internal ID15420207
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:122149296..122151830hg38UCSC Ensembl
Innerchr10:123908811..123911345hg19UCSC Ensembl
Innerchr10:123898801..123901335hg18UCSC Ensembl
Innerchr10:123898801..123901335hg17UCSC Ensembl
Cytoband10q26.13
Allele length
AssemblyAllele length
hg382535
hg192535
hg182535
hg172535
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv521165
Supporting Variants
Samples
Known GenesTACC2
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv683555
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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