A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18167897



Internal ID20734937
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:25530105..25541561hg38UCSC Ensembl
chr8:25387621..25399077hg19UCSC Ensembl
Cytoband8p21.2
Allele length
AssemblyAllele length
hg3811457
hg1911457
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6429651
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18167897
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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