A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv525085



Internal ID15105692
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:3486714..3490150hg38UCSC Ensembl
Innerchr17:3390008..3393444hg19UCSC Ensembl
Innerchr17:3336758..3340194hg18UCSC Ensembl
Innerchr17:3336758..3340194hg17UCSC Ensembl
Cytoband17p13.2
Allele length
AssemblyAllele length
hg383437
hg193437
hg183437
hg173437
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv701143
Samples
Known GenesASPA
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv525085
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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