A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3732976



Internal ID19031257
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:68669724..68698250hg38UCSC Ensembl
Innerchr3:68718875..68747401hg19UCSC Ensembl
Innerchr3:68801565..68830091hg18UCSC Ensembl
Cytoband3p14.1
Allele length
AssemblyAllele length
hg3828527
hg1928527
hg1828527
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1008984
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3732976
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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