A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv698191



Internal ID15088157
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:177187528..177282118hg38UCSC Ensembl
Innerchr5:176614529..176709119hg19UCSC Ensembl
Innerchr5:176547135..176641725hg18UCSC Ensembl
Innerchr5:176547135..176641725hg17UCSC Ensembl
Cytoband5q35.3
Allele length
AssemblyAllele length
hg3894591
hg1994591
hg1894591
hg1794591
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv521575
Supporting Variants
Samples
Known GenesNSD1
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv698191
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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