A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1155371



Internal ID22085876
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:9892135..9915653hg38UCSC Ensembl
Outerchr17:9890879..9916380hg38UCSC Ensembl
Innerchr17:9795452..9818970hg19UCSC Ensembl
Outerchr17:9794196..9819697hg19UCSC Ensembl
Cytoband17p13.1
Allele length
AssemblyAllele length
hg3825502
hg1925502
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv4010079
Samples
Known GenesGAS7, RCVRN
MethodSNP array
AnalysisDefault settings
Platform
Comments
ReferenceLou_et_al_2014
Pubmed ID25026903
Accession Number(s)nsv1155371
Frequency
Sample Size131
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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