A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6139263



Internal ID338448
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:94836431..94846503hg38UCSC Ensembl
chr3:94555275..94565347hg19UCSC Ensembl
Cytoband3q11.2
Allele length
AssemblyAllele length
hg3810073
hg1910073
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16936717
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv6139263
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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