A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18171450



Internal ID20738490
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:77339412..77351697hg38UCSC Ensembl
chr8:78251648..78263933hg19UCSC Ensembl
Cytoband8q21.11
Allele length
AssemblyAllele length
hg3812286
hg1912286
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6422261
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18171450
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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