A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18164891



Internal ID20731931
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:126197652..126198133hg38UCSC Ensembl
chr8:127209896..127210377hg19UCSC Ensembl
Cytoband8q24.13
Allele length
AssemblyAllele length
hg38482
hg19482
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6430401
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18164891
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00034


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