A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1006613



Internal ID19095830
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:18655..61275hg38UCSC Ensembl
Innerchr3:60333..102958hg19UCSC Ensembl
Innerchr3:35333..77958hg18UCSC Ensembl
Cytoband3p26.3
Allele length
AssemblyAllele length
hg3842621
hg1942626
hg1842626
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4602n100
Supporting Variantsnssv3593506, nssv3593507
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)nsv1006613
Frequency
Sample Size11257
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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