A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv528869



Internal ID15456162
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:128100617..128175412hg38UCSC Ensembl
Innerchr6:128421762..128496557hg19UCSC Ensembl
Innerchr6:128463455..128538250hg18UCSC Ensembl
Innerchr6:128463455..128538250hg17UCSC Ensembl
Cytoband6q22.33
Allele length
AssemblyAllele length
hg3874796
hg1974796
hg1874796
hg1774796
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv705549
Samples
Known GenesPTPRK
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv528869
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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