A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv837169



Internal ID16131125
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:20374016..20418791hg38UCSC Ensembl
Innerchr15:20579269..20624044hg19UCSC Ensembl
Innerchr15:18839283..18884058hg18UCSC Ensembl
Cytoband15q11.1
Allele length
AssemblyAllele length
hg3844776
hg1944776
hg1844776
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv567369
Supporting Variants
Samples
Known GenesHERC2P3
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv837169
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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