A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5460537



Internal ID238516
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:137988000..137994790hg38UCSC Ensembl
chr6:138309137..138315927hg19UCSC Ensembl
Cytoband6q23.3
Allele length
AssemblyAllele length
hg386791
hg196791
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16970157
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5460537
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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