A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv527584



Internal ID15454877
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:73816264..73816377hg38UCSC Ensembl
Innerchr17:71812403..71812516hg19UCSC Ensembl
Innerchr17:69323998..69324111hg18UCSC Ensembl
Innerchr17:69323998..69324111hg17UCSC Ensembl
Cytoband17q25.1
Allele length
AssemblyAllele length
hg38114
hg19114
hg18114
hg17114
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv704045
Samples
Known GenesLINC00469
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv527584
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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