A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1004560



Internal ID19093778
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:3676363..3725708hg38UCSC Ensembl
Innerchr3:3718047..3767392hg19UCSC Ensembl
Innerchr3:3693047..3742392hg18UCSC Ensembl
Cytoband3p26.2
Allele length
AssemblyAllele length
hg3849346
hg1949346
hg1849346
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4637n100
Supporting Variantsnssv3590388
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)nsv1004560
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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