A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5461694



Internal ID239639
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:80493063..80493178hg38UCSC Ensembl
chr6:81202780..81202895hg19UCSC Ensembl
Cytoband6q14.1
Allele length
AssemblyAllele length
hg38116
hg19116
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16985706
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5461694
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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