A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1038663



Internal ID19127882
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:57340817..57494222hg38UCSC Ensembl
Innerchr15:57633015..57786420hg19UCSC Ensembl
Innerchr15:55420307..55573712hg18UCSC Ensembl
Cytoband15q21.3
Allele length
AssemblyAllele length
hg38153406
hg19153406
hg18153406
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2607n100
Supporting Variantsnssv3717937
Samples
Known GenesCGNL1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1038663
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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