A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv574130



Internal ID16361539
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:949100..949630hg38UCSC Ensembl
Innerchr17:852340..852870hg19UCSC Ensembl
Innerchr17:799090..799620hg18UCSC Ensembl
Cytoband17p13.3
Allele length
AssemblyAllele length
hg38531
hg19531
hg18531
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5401n54
Supporting Variantsnssv866183, nssv866185, nssv866184, nssv866181, nssv866180, nssv866182, nssv866179
Samples
Known GenesNXN
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv574130
Frequency
Sample Size17421
Observed Gain0
Observed Loss7
Observed Complex0
Frequencyn/a


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