A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1023862



Internal ID19113079
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:32122490..32158337hg38UCSC Ensembl
Innerchr5:32122596..32158443hg19UCSC Ensembl
Innerchr5:32158353..32194200hg18UCSC Ensembl
Cytoband5p13.3
Allele length
AssemblyAllele length
hg3835848
hg1935848
hg1835848
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5624n100
Supporting Variantsnssv3745961
Samples
Known GenesGOLPH3
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1023862
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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