A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv575564



Internal ID16362973
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:52946005..53065715hg38UCSC Ensembl
Innerchr17:51023365..51143076hg19UCSC Ensembl
Innerchr17:48378364..48498075hg18UCSC Ensembl
Cytoband17q22
Allele length
AssemblyAllele length
hg38119711
hg19119712
hg18119712
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5692n54
Supporting Variantsnssv873551
Samples
Known GenesC17orf112
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv575564
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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