A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1042994



Internal ID19132213
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:20381394..20422227hg38UCSC Ensembl
Innerchr15:20586647..20627480hg19UCSC Ensembl
Innerchr15:18846661..18887494hg18UCSC Ensembl
Cytoband15q11.1
Allele length
AssemblyAllele length
hg3840834
hg1940834
hg1840834
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2275n100
Supporting Variantsnssv3538696
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)nsv1042994
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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