A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18210196



Internal ID20777236
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:11584151..13998677hg38UCSC Ensembl
chr4:11585775..14000301hg19UCSC Ensembl
Cytoband4p15.33
Allele length
AssemblyAllele length
hg382414527
hg192414527
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6368324
Supporting Variants
Samples
Known GenesBOD1L1, LINC01096, LINC01097, MIR5091, NKX3-2, RAB28
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18210196
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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