A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv574793



Internal ID16015516
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:36202819..36210694hg38UCSC Ensembl
Innerchr17:34530219..34538096hg19UCSC Ensembl
Innerchr17:31554332..31562209hg18UCSC Ensembl
Cytoband17q12
Allele length
AssemblyAllele length
hg387876
hg197878
hg187878
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5544n54
Supporting Variantsnssv869953, nssv869954, nssv869952, nssv869951
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv574793
Frequency
Sample Size17421
Observed Gain0
Observed Loss4
Observed Complex0
Frequencyn/a


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