A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv866460



Internal ID16160416
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:3681843..3687590hg38UCSC Ensembl
Innerchr17:3585137..3590884hg19UCSC Ensembl
Innerchr17:3531886..3537633hg18UCSC Ensembl
Cytoband17p13.2
Allele length
AssemblyAllele length
hg385748
hg195748
hg185748
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv574244
Supporting Variants
Samples
Known GenesP2RX5, P2RX5-TAX1BP3
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv866460
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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