A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6139482



Internal ID338668
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:113025100..113031680hg38UCSC Ensembl
chr3:112743947..112750527hg19UCSC Ensembl
Cytoband3q13.2
Allele length
AssemblyAllele length
hg386581
hg196581
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16938345
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv6139482
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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