A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6379412



Internal ID21036965
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:119074001..119078300hg38UCSC Ensembl
chr4:119995156..119999455hg19UCSC Ensembl
Cytoband4q26
Allele length
AssemblyAllele length
hg384300
hg194300
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5433n223
Supporting Variantsnssv18211971
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6379412
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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