A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5469602



Internal ID247383
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:85663244..85664249hg38UCSC Ensembl
chr6:86372962..86373967hg19UCSC Ensembl
Cytoband6q14.3
Allele length
AssemblyAllele length
hg381006
hg191006
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16985289
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5469602
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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