A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18167750



Internal ID20734790
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:48628164..48641909hg38UCSC Ensembl
chr8:49540724..49554469hg19UCSC Ensembl
Cytoband8q11.21
Allele length
AssemblyAllele length
hg3813746
hg1913746
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6430223
Supporting Variants
Samples
Known GenesLOC101929268
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18167750
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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