A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv575831



Internal ID16016554
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:61042000..61047056hg38UCSC Ensembl
Innerchr17:59119361..59124417hg19UCSC Ensembl
Innerchr17:56474143..56479199hg18UCSC Ensembl
Cytoband17q23.2
Allele length
AssemblyAllele length
hg385057
hg195057
hg185057
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv875718
Samples
Known GenesBCAS3
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv575831
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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