A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18167955



Internal ID20734995
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:26794263..26794774hg38UCSC Ensembl
chr8:26651780..26652291hg19UCSC Ensembl
Cytoband8p21.2
Allele length
AssemblyAllele length
hg38512
hg19512
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6434222
Supporting Variants
Samples
Known GenesADRA1A
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18167955
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00105


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