A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18172997



Internal ID20740037
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:8394005..8403872hg38UCSC Ensembl
chr8:8251515..8261382hg19UCSC Ensembl
Cytoband8p23.1
Allele length
AssemblyAllele length
hg389868
hg199868
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6417472
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18172997
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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