A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv521208



Internal ID15101815
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:8803133..8803711hg38UCSC Ensembl
Innerchr17:8706451..8707029hg19UCSC Ensembl
Innerchr17:8647176..8647754hg18UCSC Ensembl
Innerchr17:8647176..8647754hg17UCSC Ensembl
Cytoband17p13.1
Allele length
AssemblyAllele length
hg38579
hg19579
hg18579
hg17579
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv697846
Samples
Known GenesPIK3R6
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv521208
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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