A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6139425



Internal ID338610
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:35591662..35865630hg38UCSC Ensembl
chr2:35816728..36090696hg19UCSC Ensembl
Cytoband2p22.3
Allele length
AssemblyAllele length
hg38273969
hg19273969
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16911818
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv6139425
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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