A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6139648



Internal ID338837
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:113391618..113408559hg38UCSC Ensembl
chr2:114149195..114166136hg19UCSC Ensembl
Cytoband2q13
Allele length
AssemblyAllele length
hg3816942
hg1916942
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16918241
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv6139648
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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