A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1155481



Internal ID22085986
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:50233697..50242754hg38UCSC Ensembl
Outerchr17:50230336..50248951hg38UCSC Ensembl
Innerchr17:48311058..48320115hg19UCSC Ensembl
Outerchr17:48307697..48326312hg19UCSC Ensembl
Cytoband17q21.33
Allele length
AssemblyAllele length
hg3818616
hg1918616
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv143n97
Supporting Variantsnssv4011860
Samples
Known Genes
MethodSNP array
AnalysisDefault settings
Platform
Comments
ReferenceLou_et_al_2014
Pubmed ID25026903
Accession Number(s)nsv1155481
Frequency
Sample Size131
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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