A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1002625



Internal ID19091842
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:3473916..3497419hg38UCSC Ensembl
Innerchr3:3515600..3539103hg19UCSC Ensembl
Innerchr3:3490600..3514103hg18UCSC Ensembl
Cytoband3p26.2
Allele length
AssemblyAllele length
hg3823504
hg1923504
hg1823504
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3590383, nssv3590384
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)nsv1002625
Frequency
Sample Size11257
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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