A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv525225



Internal ID15452518
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:81553265..81587291hg38UCSC Ensembl
Innerchr5:80849084..80883110hg19UCSC Ensembl
Innerchr5:80884840..80918866hg18UCSC Ensembl
Innerchr5:80884840..80918866hg17UCSC Ensembl
Cytoband5q14.1
Allele length
AssemblyAllele length
hg3834027
hg1934027
hg1834027
hg1734027
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv701313
Samples
Known GenesSSBP2
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv525225
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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