A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1012634



Internal ID18755166
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:9459492..9800742hg38UCSC Ensembl
Innerchr4:9461218..9802366hg19UCSC Ensembl
Innerchr4:9070316..9411464hg18UCSC Ensembl
Cytoband4p16.1
Allele length
AssemblyAllele length
hg38341251
hg19341149
hg18341149
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5108n100
Supporting Variantsnssv3738209
Samples
Known GenesDRD5, LOC650293, MIR548I2
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1012634
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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