A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1003296



Internal ID19092515
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 StatusM
Merged Variantsdgv4672n100
Supporting Variantsnssv3591823
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)nsv1003296
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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