A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6368324



Internal ID21025877
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 StatusM
Merged Variants
Supporting Variantsnssv18210196
Samples
Known GenesBOD1L1, LINC01096, LINC01097, MIR5091, NKX3-2, RAB28
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6368324
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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