A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv575926



Internal ID16363335
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:68112848..68187221hg38UCSC Ensembl
Innerchr17:66108989..66183362hg19UCSC Ensembl
Innerchr17:63620627..63694957hg18UCSC Ensembl
Cytoband17q24.2
Allele length
AssemblyAllele length
hg3874374
hg1974374
hg1874331
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5756n54
Supporting Variantsnssv875908
Samples
Known GenesLINC00674
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv575926
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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