A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv575766



Internal ID16363175
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:58128727..58135902hg38UCSC Ensembl
Innerchr17:56206088..56213263hg19UCSC Ensembl
Innerchr17:53561087..53568262hg18UCSC Ensembl
Cytoband17q22
Allele length
AssemblyAllele length
hg387176
hg197176
hg187176
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5728n54
Supporting Variantsnssv875526
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv575766
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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