A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1151794



Internal ID15855780
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:82658618..82717637hg38UCSC Ensembl
Innerchr3:82707769..82766788hg19UCSC Ensembl
Innerchr3:82790459..82849478hg18UCSC Ensembl
Cytoband3p12.2
Allele length
AssemblyAllele length
hg3859020
hg1959020
hg1859020
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv590781
Supporting Variants
Samples1782681317_A
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1151794
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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