A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv574581



Internal ID16361990
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:20185179..20796232hg38UCSC Ensembl
Innerchr17:20088492..20699545hg19UCSC Ensembl
Innerchr17:20029084..20640137hg18UCSC Ensembl
Cytoband17p11.2
Allele length
AssemblyAllele length
hg38611054
hg19611054
hg18611054
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv868924
Samples
Known GenesCCDC144CP, CDRT15L2, KRT16P3, LGALS9B, LOC100287072, SPECC1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv574581
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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