A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv695949



Internal ID15085915
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:14611944..14622880hg38UCSC Ensembl
Innerchr11:14633490..14644426hg19UCSC Ensembl
Innerchr11:14590066..14601002hg18UCSC Ensembl
Innerchr11:14590066..14601002hg17UCSC Ensembl
Cytoband11p15.2
Allele length
AssemblyAllele length
hg3810937
hg1910937
hg1810937
hg1710937
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv518508
Supporting Variants
Samples
Known GenesPSMA1
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv695949
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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