A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1012994



Internal ID19102211
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:35762271..35905327hg38UCSC Ensembl
Innerchr3:35803763..35946819hg19UCSC Ensembl
Innerchr3:35778767..35921823hg18UCSC Ensembl
Cytoband3p22.3
Allele length
AssemblyAllele length
hg38143057
hg19143057
hg18143057
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4717n100
Supporting Variantsnssv3739687
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)nsv1012994
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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