A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv575465



Internal ID16016188
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:47545174..47552407hg38UCSC Ensembl
Innerchr17:45622540..45629773hg19UCSC Ensembl
Innerchr17:42977539..42984772hg18UCSC Ensembl
Cytoband17q21.32
Allele length
AssemblyAllele length
hg387234
hg197234
hg187234
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv873066
Samples
Known GenesNPEPPS
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv575465
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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