A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv575900



Internal ID16016623
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:66963551..66965302hg38UCSC Ensembl
Innerchr17:64959667..64961418hg19UCSC Ensembl
Innerchr17:62390129..62391880hg18UCSC Ensembl
Cytoband17q24.2
Allele length
AssemblyAllele length
hg381752
hg191752
hg181752
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv875851
Samples
Known GenesCACNG4
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv575900
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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