A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv698122



Internal ID15434774
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:86727073..86804030hg38UCSC Ensembl
Innerchr11:86438115..86515072hg19UCSC Ensembl
Innerchr11:86115763..86192720hg18UCSC Ensembl
Innerchr11:86115763..86192720hg17UCSC Ensembl
Cytoband11q14.2
Allele length
AssemblyAllele length
hg3876958
hg1976958
hg1876958
hg1776958
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv521505
Supporting Variants
Samples
Known GenesPRSS23
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv698122
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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