A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6140191



Internal ID339383
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:3597552..3711776hg38UCSC Ensembl
chr4:3599279..3713503hg19UCSC Ensembl
Cytoband4p16.3
Allele length
AssemblyAllele length
hg38114225
hg19114225
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16945704
Samples
Known GenesLOC100133461
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv6140191
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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