A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv525596



Internal ID15106203
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:83926497..83979269hg38UCSC Ensembl
Innerchr5:83222316..83275088hg19UCSC Ensembl
Innerchr5:83258072..83310844hg18UCSC Ensembl
Innerchr5:83258072..83310844hg17UCSC Ensembl
Cytoband5q14.3
Allele length
AssemblyAllele length
hg3852773
hg1952773
hg1852773
hg1752773
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv701739
Samples
Known GenesEDIL3
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv525596
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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