A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5463696



Internal ID241591
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:37819225..37819344hg38UCSC Ensembl
chr6:37787001..37787120hg19UCSC Ensembl
Cytoband6p21.2
Allele length
AssemblyAllele length
hg38120
hg19120
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16980595
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5463696
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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