A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1012374



Internal ID19101591
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:35759275..35892079hg38UCSC Ensembl
Innerchr3:35800767..35933571hg19UCSC Ensembl
Innerchr3:35775771..35908575hg18UCSC Ensembl
Cytoband3p22.3
Allele length
AssemblyAllele length
hg38132805
hg19132805
hg18132805
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4717n100
Supporting Variantsnssv3739674
Samples
Known GenesARPP21
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1012374
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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