A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18170382



Internal ID20737422
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:77402407..77402754hg38UCSC Ensembl
chr8:78314643..78314990hg19UCSC Ensembl
Cytoband8q21.12
Allele length
AssemblyAllele length
hg38348
hg19348
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6433563
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18170382
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00128


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