A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv527550



Internal ID15454843
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:72484960..72494101hg38UCSC Ensembl
Innerchr17:70481100..70490241hg19UCSC Ensembl
Innerchr17:67992695..68001836hg18UCSC Ensembl
Innerchr17:67992695..68001836hg17UCSC Ensembl
Cytoband17q24.3
Allele length
AssemblyAllele length
hg389142
hg199142
hg189142
hg179142
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv704011
Samples
Known GenesLINC00673
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv527550
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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