A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv525993



Internal ID15453286
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:108952644..108964043hg38UCSC Ensembl
Innerchr5:108288345..108299744hg19UCSC Ensembl
Innerchr5:108316244..108327643hg18UCSC Ensembl
Innerchr5:108316244..108327643hg17UCSC Ensembl
Cytoband5q21.3
Allele length
AssemblyAllele length
hg3811400
hg1911400
hg1811400
hg1711400
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv702218
Samples
Known GenesFER
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv525993
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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