A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv866333



Internal ID16160289
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:1052582..1053226hg38UCSC Ensembl
Innerchr17:955822..956466hg19UCSC Ensembl
Innerchr17:902572..903216hg18UCSC Ensembl
Cytoband17p13.3
Allele length
AssemblyAllele length
hg38645
hg19645
hg18645
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv574167
Supporting Variants
Samples
Known GenesABR
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv866333
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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