A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1040164



Internal ID19129383
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:19811063..20060713hg38UCSC Ensembl
Innerchr15:20016316..20265966hg19UCSC Ensembl
Innerchr15:18276329..18525980hg18UCSC Ensembl
Cytoband15q11.1
Allele length
AssemblyAllele length
hg38249651
hg19249651
hg18249652
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2172n100
Supporting Variantsnssv3534420, nssv3534421, nssv3534422
Samples
Known Genes
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1040164
Frequency
Sample Size11257
Observed Gain3
Observed Loss0
Observed Complex0
Frequencyn/a


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