A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5465915



Internal ID243767
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:80400974..80401175hg38UCSC Ensembl
chr6:81110691..81110892hg19UCSC Ensembl
Cytoband6q14.1
Allele length
AssemblyAllele length
hg38202
hg19202
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16985697
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5465915
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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