A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv575837



Internal ID16016560
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:61044669..61051300hg38UCSC Ensembl
Innerchr17:59122030..59128661hg19UCSC Ensembl
Innerchr17:56476812..56483443hg18UCSC Ensembl
Cytoband17q23.2
Allele length
AssemblyAllele length
hg386632
hg196632
hg186632
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5739n54
Supporting Variantsnssv875738
Samples
Known GenesBCAS3
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv575837
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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