A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv524219



Internal ID15451512
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:96890148..96914405hg38UCSC Ensembl
Innerchr4:97811299..97835556hg19UCSC Ensembl
Innerchr4:98030322..98054579hg18UCSC Ensembl
Innerchr4:98168477..98192734hg17UCSC Ensembl
Cytoband4q22.3
Allele length
AssemblyAllele length
hg3824258
hg1924258
hg1824258
hg1724258
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv700107
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv524219
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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