A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv525851



Internal ID15106458
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:77334838..77354790hg38UCSC Ensembl
Innerchr17:75330920..75350872hg19UCSC Ensembl
Innerchr17:72842515..72862467hg18UCSC Ensembl
Innerchr17:72842515..72862467hg17UCSC Ensembl
Cytoband17q25.2
Allele length
AssemblyAllele length
hg3819953
hg1919953
hg1819953
hg1719953
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv702045
Samples
Known GenesSEPT9
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv525851
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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