A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv525272



Internal ID15452565
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:142630815..142640943hg38UCSC Ensembl
Innerchr5:142010380..142020508hg19UCSC Ensembl
Innerchr5:141990564..142000692hg18UCSC Ensembl
Innerchr5:141990564..142000692hg17UCSC Ensembl
Cytoband5q31.3
Allele length
AssemblyAllele length
hg3810129
hg1910129
hg1810129
hg1710129
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv701373
Samples
Known GenesFGF1
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv525272
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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