A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18164751



Internal ID20731791
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:134765473..134783592hg38UCSC Ensembl
chr8:135777716..135795835hg19UCSC Ensembl
Cytoband8q24.22
Allele length
AssemblyAllele length
hg3818120
hg1918120
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6419018
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18164751
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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