A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv528074



Internal ID15455367
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:40913201..40915982hg38UCSC Ensembl
Innerchr17:39069453..39072234hg19UCSC Ensembl
Innerchr17:36322979..36325760hg18UCSC Ensembl
Innerchr17:36322979..36325760hg17UCSC Ensembl
Cytoband17q21.2
Allele length
AssemblyAllele length
hg382782
hg192782
hg182782
hg172782
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv704610
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv528074
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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