A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18167439



Internal ID20734479
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:35943613..35953235hg38UCSC Ensembl
chr8:35801131..35810753hg19UCSC Ensembl
Cytoband8p12
Allele length
AssemblyAllele length
hg389623
hg199623
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6429736
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18167439
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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