A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv694188



Internal ID15084154
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:14620336..14668646hg38UCSC Ensembl
Innerchr11:14641882..14690192hg19UCSC Ensembl
Innerchr11:14598458..14646768hg18UCSC Ensembl
Innerchr11:14598458..14646768hg17UCSC Ensembl
Cytoband11p15.2
Allele length
AssemblyAllele length
hg3848311
hg1948311
hg1848311
hg1748311
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv517985
Supporting Variants
Samples
Known GenesPDE3B, PSMA1
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv694188
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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