A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv976729



Internal ID15923999
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:150015043..150047998hg38UCSC Ensembl
Innerchr3:149732830..149765785hg19UCSC Ensembl
Innerchr3:151215520..151248475hg18UCSC Ensembl
Cytoband3q25.1
Allele length
AssemblyAllele length
hg3832956
hg1932956
hg1832956
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv592032
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)nssv976729
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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