A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv965586



Internal ID16259542
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:72732656..72734985hg38UCSC Ensembl
Innerchr3:72781807..72784136hg19UCSC Ensembl
Innerchr3:72864497..72866826hg18UCSC Ensembl
Cytoband3p13
Allele length
AssemblyAllele length
hg382330
hg192330
hg182330
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv590629
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)nssv965586
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer