A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv575558



Internal ID16362967
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:52874219..53236604hg38UCSC Ensembl
Innerchr17:50951579..51313965hg19UCSC Ensembl
Innerchr17:48306578..48668964hg18UCSC Ensembl
Cytoband17q22
Allele length
AssemblyAllele length
hg38362386
hg19362387
hg18362387
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5691n54
Supporting Variantsnssv873545
Samples
Known GenesC17orf112
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv575558
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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