A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16984516



Internal ID57063
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:69753503..69757851hg38UCSC Ensembl
chr6:70463395..70467743hg19UCSC Ensembl
Cytoband6q13
Allele length
AssemblyAllele length
hg384349
hg194349
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5463501
Supporting Variants
Samples
Known GenesLMBRD1
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16984516
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000468


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