A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18162052



Internal ID20729092
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:106760557..106808649hg38UCSC Ensembl
chr8:107772785..107820877hg19UCSC Ensembl
Cytoband8q23.1
Allele length
AssemblyAllele length
hg3848093
hg1948093
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6415909
Supporting Variants
Samples
Known GenesABRA
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18162052
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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