A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6143594



Internal ID342795
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:24677277..24689130hg38UCSC Ensembl
chr11:24698823..24710676hg19UCSC Ensembl
Cytoband11p14.3
Allele length
AssemblyAllele length
hg3811854
hg1911854
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17044944
Samples
Known GenesLUZP2
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv6143594
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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