A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1042371



Internal ID19131590
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:20344625..20441310hg38UCSC Ensembl
Innerchr15:20549878..20646563hg19UCSC Ensembl
Innerchr15:18809892..18906577hg18UCSC Ensembl
Cytoband15q11.1
Allele length
AssemblyAllele length
hg3896686
hg1996686
hg1896686
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2248n100
Supporting Variantsnssv3536296, nssv3536295
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)nsv1042371
Frequency
Sample Size11257
Observed Gain1
Observed Loss1
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer