A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv658661



Internal ID15395313
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:135279325..135296324hg38UCSC Ensembl
Innerchr5:134615015..134632014hg19UCSC Ensembl
Innerchr5:134642914..134659913hg18UCSC Ensembl
Innerchr5:134642914..134659913hg17UCSC Ensembl
Cytoband5q31.1
Allele length
AssemblyAllele length
hg3817000
hg1917000
hg1817000
hg1717000
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv519790
Supporting Variants
Samples
Known GenesC5orf66
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv658661
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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