A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv526257



Internal ID15453550
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:136507618..136542736hg38UCSC Ensembl
Innerchr4:137428773..137463891hg19UCSC Ensembl
Innerchr4:137648223..137683341hg18UCSC Ensembl
Innerchr4:137786378..137821496hg17UCSC Ensembl
Cytoband4q28.3
Allele length
AssemblyAllele length
hg3835119
hg1935119
hg1835119
hg1735119
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv702529
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv526257
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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