A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18171767



Internal ID20738807
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:93825501..93828000hg38UCSC Ensembl
chr8:94837729..94840228hg19UCSC Ensembl
Cytoband8q22.1
Allele length
AssemblyAllele length
hg382500
hg192500
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6418156
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18171767
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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