A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1040544



Internal ID19129763
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:20327352..20422227hg38UCSC Ensembl
Innerchr15:20532605..20627480hg19UCSC Ensembl
Innerchr15:18792619..18887494hg18UCSC Ensembl
Cytoband15q11.1
Allele length
AssemblyAllele length
hg3894876
hg1994876
hg1894876
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2242n100
Supporting Variantsnssv3536155, nssv3536157, nssv3536156, nssv3536153, nssv3536154
Samples
Known GenesHERC2P3
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1040544
Frequency
Sample Size11257
Observed Gain4
Observed Loss1
Observed Complex0
Frequencyn/a


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