A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv4011859



Internal ID22073490
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:50233697..50240990hg38UCSC Ensembl
Outerchr17:50230336..50242754hg38UCSC Ensembl
Innerchr17:48311058..48318351hg19UCSC Ensembl
Outerchr17:48307697..48320115hg19UCSC Ensembl
Cytoband17q21.33
Allele length
AssemblyAllele length
hg3812419
hg1912419
Variant TypeCNV deletion
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1155480
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisDefault settings
Platform
Comments
ReferenceLou_et_al_2014
Pubmed ID25026903
Accession Number(s)nssv4011859
Frequency
Sample Size131
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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