A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv703132



Internal ID15439784
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:777799..792613hg38UCSC Ensembl
Innerchr4:771587..786401hg19UCSC Ensembl
Innerchr4:761587..776401hg18UCSC Ensembl
Innerchr4:761417..776231hg17UCSC Ensembl
Cytoband4p16.3
Allele length
AssemblyAllele length
hg3814815
hg1914815
hg1814815
hg1714815
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv526780
Supporting Variants
Samples
Known GenesCPLX1, LOC100129917
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv703132
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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