A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5461722



Internal ID239668
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:71561449..71563556hg38UCSC Ensembl
chr6:72271152..72273259hg19UCSC Ensembl
Cytoband6q13
Allele length
AssemblyAllele length
hg382108
hg192108
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16987192
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5461722
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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