A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5464861



Internal ID242733
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:98085882..98089206hg38UCSC Ensembl
chr6:98533758..98537082hg19UCSC Ensembl
Cytoband6q16.1
Allele length
AssemblyAllele length
hg383325
hg193325
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16985216
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5464861
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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