A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18173562



Internal ID20740602
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:97777429..97781281hg38UCSC Ensembl
chr8:98789657..98793509hg19UCSC Ensembl
Cytoband8q22.1
Allele length
AssemblyAllele length
hg383853
hg193853
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6431602
Supporting Variants
Samples
Known GenesLAPTM4B
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18173562
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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