A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5465588



Internal ID243448
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:1142931..1213747hg38UCSC Ensembl
chr6:1143166..1213982hg19UCSC Ensembl
Cytoband6p25.3
Allele length
AssemblyAllele length
hg3870817
hg1970817
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16979877
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5465588
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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