A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv749776



Internal ID16043732
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:65597778..65633179hg38UCSC Ensembl
Innerchr10:67357536..67392937hg19UCSC Ensembl
Innerchr10:67027542..67062943hg18UCSC Ensembl
Cytoband10q21.3
Allele length
AssemblyAllele length
hg3835402
hg1935402
hg1835402
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv551288
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)nssv749776
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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