A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv749777



Internal ID16043733
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:65662026..65714631hg38UCSC Ensembl
Innerchr10:67421784..67474389hg19UCSC Ensembl
Innerchr10:67091790..67144395hg18UCSC Ensembl
Cytoband10q21.3
Allele length
AssemblyAllele length
hg3852606
hg1952606
hg1852606
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv551289
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)nssv749777
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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