A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1039582



Internal ID19128801
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:20359322..20525214hg38UCSC Ensembl
Innerchr15:20564575..20730453hg19UCSC Ensembl
Innerchr15:18824589..18990467hg18UCSC Ensembl
Cytoband15q11.1
Allele length
AssemblyAllele length
hg38165893
hg19165879
hg18165879
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2243n100
Supporting Variantsnssv3537540, nssv3713780, nssv3537541, nssv3713781, nssv3537539
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)nsv1039582
Frequency
Sample Size11257
Observed Gain4
Observed Loss1
Observed Complex0
Frequencyn/a


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