A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv998218



Internal ID19157755
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:73109319..73177882hg38UCSC Ensembl
Innerchr3:73158470..73227033hg19UCSC Ensembl
Innerchr3:73241160..73309723hg18UCSC Ensembl
Cytoband3p13
Allele length
AssemblyAllele length
hg3868564
hg1968564
hg1868564
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3594161
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)nsv998218
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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