A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6139352



Internal ID338537
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:198185574..198192000hg38UCSC Ensembl
chr3:197912445..197918871hg19UCSC Ensembl
Cytoband3q29
Allele length
AssemblyAllele length
hg386427
hg196427
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16944633
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv6139352
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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