A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv748563



Internal ID16042519
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:56697251..56942680hg38UCSC Ensembl
Innerchr10:58457011..58702440hg19UCSC Ensembl
Innerchr10:58127017..58372446hg18UCSC Ensembl
Cytoband10q21.1
Allele length
AssemblyAllele length
hg38245430
hg19245430
hg18245430
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv551064
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)nssv748563
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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