A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv573950



Internal ID16361359
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:220894..221936hg38UCSC Ensembl
Innerchr17:70685..71727hg19UCSC Ensembl
Innerchr17:70685..71727hg18UCSC Ensembl
Cytoband17p13.3
Allele length
AssemblyAllele length
hg381043
hg191043
hg181043
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv864408
Samples
Known GenesRPH3AL
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv573950
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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