A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6424570



Internal ID21082123
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:97777301..97790547hg38UCSC Ensembl
chr8:98789529..98802775hg19UCSC Ensembl
Cytoband8q22.1
Allele length
AssemblyAllele length
hg3813247
hg1913247
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18217614
Samples
Known GenesLAPTM4B
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6424570
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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