A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5458733



Internal ID236753
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:36948965..36950669hg38UCSC Ensembl
chr6:36916741..36918445hg19UCSC Ensembl
Cytoband6p21.2
Allele length
AssemblyAllele length
hg381705
hg191705
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16982098
Samples
Known GenesPI16
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5458733
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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