A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv998847



Internal ID19158384
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:46760315..46771570hg38UCSC Ensembl
Innerchr3:46801805..46813060hg19UCSC Ensembl
Innerchr3:46776809..46788064hg18UCSC Ensembl
Cytoband3p21.31
Allele length
AssemblyAllele length
hg3811256
hg1911256
hg1811256
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3590977, nssv3590976
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)nsv998847
Frequency
Sample Size11257
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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