A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1043741



Internal ID19132960
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:28666612..28697547hg38UCSC Ensembl
Innerchr15:28911758..28942693hg19UCSC Ensembl
Innerchr15:26710799..26741734hg18UCSC Ensembl
Cytoband15q13.1
Allele length
AssemblyAllele length
hg3830936
hg1930936
hg1830936
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2493n100
Supporting Variantsnssv3721474
Samples
Known GenesHERC2P9
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1043741
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