A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18170871



Internal ID20737911
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:8934700..8982079hg38UCSC Ensembl
chr8:8792210..8839589hg19UCSC Ensembl
Cytoband8p23.1
Allele length
AssemblyAllele length
hg3847380
hg1947380
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6421319
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18170871
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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