A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv688362



Internal ID15425014
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:161024150..161081425hg38UCSC Ensembl
Innerchr4:161945302..162002577hg19UCSC Ensembl
Innerchr4:162164752..162222027hg18UCSC Ensembl
Innerchr4:162302907..162360182hg17UCSC Ensembl
Cytoband4q32.2
Allele length
AssemblyAllele length
hg3857276
hg1957276
hg1857276
hg1757276
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv515755
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv688362
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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