A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3591823



Internal ID18890104
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:6601808..6613379hg38UCSC Ensembl
Innerchr3:6643495..6655066hg19UCSC Ensembl
Innerchr3:6618495..6630066hg18UCSC Ensembl
Cytoband3p26.1
Allele length
AssemblyAllele length
hg3811572
hg1911572
hg1811572
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1003296
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)nssv3591823
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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