A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv574118



Internal ID16361527
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:948992..949579hg38UCSC Ensembl
Innerchr17:852232..852819hg19UCSC Ensembl
Innerchr17:798982..799569hg18UCSC Ensembl
Cytoband17p13.3
Allele length
AssemblyAllele length
hg38588
hg19588
hg18588
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5398n54
Supporting Variantsnssv866113, nssv866117, nssv866111, nssv866110, nssv866114, nssv866116, nssv866112, nssv866115
Samples
Known GenesNXN
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv574118
Frequency
Sample Size17421
Observed Gain0
Observed Loss8
Observed Complex0
Frequencyn/a


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