A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv752188



Internal ID16046144
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:84840324..85032590hg38UCSC Ensembl
Innerchr10:86600080..86792346hg19UCSC Ensembl
Innerchr10:86590060..86782326hg18UCSC Ensembl
Cytoband10q23.1
Allele length
AssemblyAllele length
hg38192267
hg19192267
hg18192267
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv551759
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)nssv752188
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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