A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6438764



Internal ID21096317
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:6409642..6409837hg38UCSC Ensembl
chr11:6430872..6431067hg19UCSC Ensembl
Cytoband11p15.4
Allele length
AssemblyAllele length
hg38196
hg19196
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17993836
Samples
Known GenesAPBB1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6438764
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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