A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv746834



Internal ID16040790
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:33799125..33923116hg38UCSC Ensembl
Innerchr10:34088053..34212044hg19UCSC Ensembl
Innerchr10:34128059..34252050hg18UCSC Ensembl
Cytoband10p11.22
Allele length
AssemblyAllele length
hg38123992
hg19123992
hg18123992
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv550388
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv746834
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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