A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18171772



Internal ID20738812
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:93888994..93899921hg38UCSC Ensembl
chr8:94901222..94912149hg19UCSC Ensembl
Cytoband8q22.1
Allele length
AssemblyAllele length
hg3810928
hg1910928
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6433953
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18171772
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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