A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv575565



Internal ID16362974
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:52946005..53228656hg38UCSC Ensembl
Innerchr17:51023365..51306017hg19UCSC Ensembl
Innerchr17:48378364..48661016hg18UCSC Ensembl
Cytoband17q22
Allele length
AssemblyAllele length
hg38282652
hg19282653
hg18282653
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5691n54
Supporting Variantsnssv873552
Samples
Known GenesC17orf112
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv575565
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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