A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv749380



Internal ID16043336
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:65503491..65576927hg38UCSC Ensembl
Innerchr10:67263249..67336685hg19UCSC Ensembl
Innerchr10:66933255..67006691hg18UCSC Ensembl
Cytoband10q21.3
Allele length
AssemblyAllele length
hg3873437
hg1973437
hg1873437
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv551252
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)nssv749380
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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