A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv746944



Internal ID16040900
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:38576045..38672001hg38UCSC Ensembl
Innerchr10:38869176..38965132hg19UCSC Ensembl
Innerchr10:38909182..39005138hg18UCSC Ensembl
Cytoband10p11.1
Allele length
AssemblyAllele length
hg3895957
hg1995957
hg1895957
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv550473
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)nssv746944
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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