A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6387780



Internal ID21045333
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:60123201..60127400hg38UCSC Ensembl
chr4:60988919..60993118hg19UCSC Ensembl
Cytoband4q13.1
Allele length
AssemblyAllele length
hg384200
hg194200
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18210883
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6387780
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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