A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv574850



Internal ID16015573
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:36190840..36195497hg38UCSC Ensembl
Innerchr17:34606289..34610939hg19UCSC Ensembl
Innerchr17:31630402..31635052hg18UCSC Ensembl
Cytoband17q12
Allele length
AssemblyAllele length
hg384658
hg194651
hg184651
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5557n54
Supporting Variantsnssv870063, nssv870064, nssv870062
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv574850
Frequency
Sample Size17421
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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