A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv744280



Internal ID16038236
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:18704374..18729013hg38UCSC Ensembl
Innerchr10:18993303..19017942hg19UCSC Ensembl
Innerchr10:19033309..19057948hg18UCSC Ensembl
Cytoband10p12.31
Allele length
AssemblyAllele length
hg3824640
hg1924640
hg1824640
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv550122
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)nssv744280
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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