A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv703308



Internal ID15439960
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:122089950..122090090hg38UCSC Ensembl
Innerchr10:123849465..123849605hg19UCSC Ensembl
Innerchr10:123839455..123839595hg18UCSC Ensembl
Innerchr10:123839455..123839595hg17UCSC Ensembl
Cytoband10q26.13
Allele length
AssemblyAllele length
hg38141
hg19141
hg18141
hg17141
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv526940
Supporting Variants
Samples
Known GenesTACC2
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv703308
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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