A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv574526



Internal ID16015249
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:17519294..17541055hg38UCSC Ensembl
Innerchr17:17422608..17444369hg19UCSC Ensembl
Innerchr17:17363333..17385094hg18UCSC Ensembl
Cytoband17p11.2
Allele length
AssemblyAllele length
hg3821762
hg1921762
hg1821762
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv868860
Samples
Known GenesPEMT
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv574526
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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