A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv746981



Internal ID16040937
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:38577517..38697624hg38UCSC Ensembl
Innerchr10:38870648..38990755hg19UCSC Ensembl
Innerchr10:38910654..39030761hg18UCSC Ensembl
Cytoband10p11.1
Allele length
AssemblyAllele length
hg38120108
hg19120108
hg18120108
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv550496
Supporting Variants
Samples
Known GenesACTR3BP5
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv746981
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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