A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv574111



Internal ID16361520
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:948888..952834hg38UCSC Ensembl
Innerchr17:852128..856074hg19UCSC Ensembl
Innerchr17:798878..802824hg18UCSC Ensembl
Cytoband17p13.3
Allele length
AssemblyAllele length
hg383947
hg193947
hg183947
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5397n54
Supporting Variantsnssv866089, nssv866090
Samples
Known GenesNXN
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv574111
Frequency
Sample Size17421
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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