A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv866232



Internal ID16160188
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:949100..952193hg38UCSC Ensembl
Innerchr17:852340..855433hg19UCSC Ensembl
Innerchr17:799090..802183hg18UCSC Ensembl
Cytoband17p13.3
Allele length
AssemblyAllele length
hg383094
hg193094
hg183094
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv574134
Supporting Variants
Samples
Known GenesNXN
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv866232
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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