A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv706088



Internal ID15442740
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:5503406..5552407hg38UCSC Ensembl
Innerchr4:5505133..5554134hg19UCSC Ensembl
Innerchr4:5556034..5605035hg18UCSC Ensembl
Innerchr4:5623205..5672206hg17UCSC Ensembl
Cytoband4p16.1
Allele length
AssemblyAllele length
hg3849002
hg1949002
hg1849002
hg1749002
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv522680
Supporting Variants
Samples
Known GenesC4orf6
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv706088
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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