A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18172695



Internal ID20739735
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:86293001..86317500hg38UCSC Ensembl
chr8:87305230..87329729hg19UCSC Ensembl
Cytoband8q21.3
Allele length
AssemblyAllele length
hg3824500
hg1924500
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6428592
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18172695
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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