A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv525396



Internal ID15452689
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:134517569..134626139hg38UCSC Ensembl
Innerchr4:135438724..135547294hg19UCSC Ensembl
Innerchr4:135658174..135766744hg18UCSC Ensembl
Innerchr4:135796329..135904899hg17UCSC Ensembl
Cytoband4q28.3
Allele length
AssemblyAllele length
hg38108571
hg19108571
hg18108571
hg17108571
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv701519
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv525396
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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