A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv679239



Internal ID15415891
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:39874119..39906880hg38UCSC Ensembl
Innerchr4:39875739..39908500hg19UCSC Ensembl
Innerchr4:39552134..39584895hg18UCSC Ensembl
Innerchr4:39698305..39731066hg17UCSC Ensembl
Cytoband4p14
Allele length
AssemblyAllele length
hg3832762
hg1932762
hg1832762
hg1732762
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv520312
Supporting Variants
Samples
Known GenesPDS5A
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv679239
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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