A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6140491



Internal ID339684
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:69749425..69750083hg38UCSC Ensembl
chr6:70459317..70459975hg19UCSC Ensembl
Cytoband6q13
Allele length
AssemblyAllele length
hg38659
hg19659
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16984512
Samples
Known GenesLMBRD1
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv6140491
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer