A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1000600



Internal ID19089817
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:162153428..162234318hg38UCSC Ensembl
Innerchr3:161871216..161952106hg19UCSC Ensembl
Innerchr3:163353910..163434800hg18UCSC Ensembl
Cytoband3q26.1
Allele length
AssemblyAllele length
hg3880891
hg1980891
hg1880891
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4932n100
Supporting Variantsnssv3607916, nssv3607915, nssv3607914
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)nsv1000600
Frequency
Sample Size11257
Observed Gain3
Observed Loss0
Observed Complex0
Frequencyn/a


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