A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5453943



Internal ID232052
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:63440725..63442389hg38UCSC Ensembl
chr6:64150630..64152294hg19UCSC Ensembl
Cytoband6q12
Allele length
AssemblyAllele length
hg381665
hg191665
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16984401
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5453943
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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