A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5458731



Internal ID236751
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:73202190..73204922hg38UCSC Ensembl
chr6:73911913..73914645hg19UCSC Ensembl
Cytoband6q13
Allele length
AssemblyAllele length
hg382733
hg192733
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16984593
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5458731
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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