A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv575658



Internal ID16363067
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:54568502..54886696hg38UCSC Ensembl
Innerchr17:52645863..52964057hg19UCSC Ensembl
Innerchr17:50000862..50319056hg18UCSC Ensembl
Cytoband17q22
Allele length
AssemblyAllele length
hg38318195
hg19318195
hg18318195
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv874072
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv575658
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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