A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv692598



Internal ID15429250
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:90737555..90966658hg38UCSC Ensembl
Innerchr5:90033372..90262475hg19UCSC Ensembl
Innerchr5:90069128..90298231hg18UCSC Ensembl
Innerchr5:90069128..90298231hg17UCSC Ensembl
Cytoband5q14.3
Allele length
AssemblyAllele length
hg38229104
hg19229104
hg18229104
hg17229104
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv517049
Supporting Variants
Samples
Known GenesGPR98
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv692598
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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