A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1002833



Internal ID19092050
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:65203548..65224628hg38UCSC Ensembl
Innerchr3:65189223..65210303hg19UCSC Ensembl
Innerchr3:65164263..65185343hg18UCSC Ensembl
Cytoband3p14.1
Allele length
AssemblyAllele length
hg3821081
hg1921081
hg1821081
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4761n100
Supporting Variantsnssv3592446, nssv3592447, nssv3732839
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)nsv1002833
Frequency
Sample Size11257
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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