A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1003117



Internal ID19092334
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:37280022..37354902hg38UCSC Ensembl
Innerchr3:37321513..37396393hg19UCSC Ensembl
Innerchr3:37296517..37371397hg18UCSC Ensembl
Cytoband3p22.2
Allele length
AssemblyAllele length
hg3874881
hg1974881
hg1874881
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3589675
Samples
Known GenesGOLGA4
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1003117
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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