A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv575764



Internal ID16363173
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:58125533..58135442hg38UCSC Ensembl
Innerchr17:56202894..56212803hg19UCSC Ensembl
Innerchr17:53557893..53567802hg18UCSC Ensembl
Cytoband17q22
Allele length
AssemblyAllele length
hg389910
hg199910
hg189910
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5727n54
Supporting Variantsnssv875524
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv575764
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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