A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv526250



Internal ID15453543
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:52287063..52299444hg38UCSC Ensembl
Innerchr4:53153229..53165610hg19UCSC Ensembl
Innerchr4:52847986..52860367hg18UCSC Ensembl
Innerchr4:52994157..53006538hg17UCSC Ensembl
Cytoband4q12
Allele length
AssemblyAllele length
hg3812382
hg1912382
hg1812382
hg1712382
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv702522
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv526250
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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