A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv656925



Internal ID15046891
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:188014029..188212954hg38UCSC Ensembl
Innerchr4:188935183..189134108hg19UCSC Ensembl
Innerchr4:189172177..189371102hg18UCSC Ensembl
Innerchr4:189310332..189509257hg17UCSC Ensembl
Cytoband4q35.2
Allele length
AssemblyAllele length
hg38198926
hg19198926
hg18198926
hg17198926
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv519300
Supporting Variants
Samples
Known GenesTRIML1, TRIML2
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv656925
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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