A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv864406



Internal ID15811676
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:201297..421142hg38UCSC Ensembl
Innerchr17:51088..270933hg19UCSC Ensembl
Innerchr17:51088..271176hg18UCSC Ensembl
Cytoband17p13.3
Allele length
AssemblyAllele length
hg38219846
hg19219846
hg18220089
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv573947
Supporting Variants
Samples
Known GenesC17orf97, LOC100506388, RPH3AL
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv864406
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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