A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv527709



Internal ID15108316
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:4153248..4160440hg38UCSC Ensembl
Innerchr17:4056542..4063734hg19UCSC Ensembl
Innerchr17:4003291..4010483hg18UCSC Ensembl
Innerchr17:4003291..4010483hg17UCSC Ensembl
Cytoband17p13.2
Allele length
AssemblyAllele length
hg387193
hg197193
hg187193
hg177193
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv704189
Samples
Known GenesCYB5D2
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv527709
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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