A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv999102



Internal ID18811952
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:9631623..9792557hg38UCSC Ensembl
Innerchr4:9633247..9794181hg19UCSC Ensembl
Innerchr4:9242345..9403279hg18UCSC Ensembl
Cytoband4p16.1
Allele length
AssemblyAllele length
hg38160935
hg19160935
hg18160935
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3738213
Samples
Known GenesDRD5
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv999102
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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