A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1005256



Internal ID19094473
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:65213280..65237719hg38UCSC Ensembl
Innerchr3:65198955..65223394hg19UCSC Ensembl
Innerchr3:65173995..65198434hg18UCSC Ensembl
Cytoband3p14.1
Allele length
AssemblyAllele length
hg3824440
hg1924440
hg1824440
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4768n100
Supporting Variantsnssv3593953
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)nsv1005256
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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