A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18171898



Internal ID20738938
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:81201952..81205906hg38UCSC Ensembl
chr8:82114187..82118141hg19UCSC Ensembl
Cytoband8q21.13
Allele length
AssemblyAllele length
hg383955
hg193955
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6415757
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18171898
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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