A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6406824



Internal ID21064377
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:69680252..69680986hg38UCSC Ensembl
chr6:70390144..70390878hg19UCSC Ensembl
Cytoband6q13
Allele length
AssemblyAllele length
hg38735
hg19735
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18144379
Samples
Known GenesLMBRD1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6406824
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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