A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv524539



Internal ID15451832
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:6458468..6469949hg38UCSC Ensembl
Innerchr17:6361788..6373269hg19UCSC Ensembl
Innerchr17:6302512..6313993hg18UCSC Ensembl
Innerchr17:6302512..6313993hg17UCSC Ensembl
Cytoband17p13.2
Allele length
AssemblyAllele length
hg3811482
hg1911482
hg1811482
hg1711482
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv700489
Samples
Known GenesPITPNM3
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv524539
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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