A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6139489



Internal ID338675
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:4110265..4236918hg38UCSC Ensembl
chr3:4151949..4278602hg19UCSC Ensembl
Cytoband3p26.1
Allele length
AssemblyAllele length
hg38126654
hg19126654
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv339n206
Supporting Variantsnssv16929295
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv6139489
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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