A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5467095



Internal ID244916
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:37157965..37158270hg38UCSC Ensembl
chr6:37125741..37126046hg19UCSC Ensembl
Cytoband6p21.2
Allele length
AssemblyAllele length
hg38306
hg19306
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17735521
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5467095
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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