A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1037947



Internal ID19127166
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:20327352..20441310hg38UCSC Ensembl
Innerchr15:20532605..20646563hg19UCSC Ensembl
Innerchr15:18792619..18906577hg18UCSC Ensembl
Cytoband15q11.1
Allele length
AssemblyAllele length
hg38113959
hg19113959
hg18113959
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2230n100
Supporting Variantsnssv3536158, nssv3713718
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)nsv1037947
Frequency
Sample Size11257
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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