A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6428777



Internal ID21086330
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:97849837..97851081hg38UCSC Ensembl
chr8:98862065..98863309hg19UCSC Ensembl
Cytoband8q22.1
Allele length
AssemblyAllele length
hg381245
hg191245
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18173570
Samples
Known GenesLAPTM4B
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6428777
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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