A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv575832



Internal ID16016555
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:61042000..61049006hg38UCSC Ensembl
Innerchr17:59119361..59126367hg19UCSC Ensembl
Innerchr17:56474143..56481149hg18UCSC Ensembl
Cytoband17q23.2
Allele length
AssemblyAllele length
hg387007
hg197007
hg187007
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5738n54
Supporting Variantsnssv875719, nssv875720
Samples
Known GenesBCAS3
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv575832
Frequency
Sample Size17421
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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