A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv696187



Internal ID15086153
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:189789982..189970548hg38UCSC Ensembl
Innerchr4:190711136..190891703hg19UCSC Ensembl
Innerchr4:190948130..191128697hg18UCSC Ensembl
Innerchr4:191086285..191266852hg17UCSC Ensembl
Cytoband4q35.2
Allele length
AssemblyAllele length
hg38180567
hg19180568
hg18180568
hg17180568
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv517295
Supporting Variants
Samples
Known GenesFRG1, LOC283788
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv696187
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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