A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18173491



Internal ID20740531
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:92857580..92859015hg38UCSC Ensembl
chr8:93869808..93871243hg19UCSC Ensembl
Cytoband8q22.1
Allele length
AssemblyAllele length
hg381436
hg191436
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6424280
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18173491
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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