A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv526940



Internal ID15454233
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 State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv703308
Samples
Known GenesTACC2
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv526940
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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