A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18173706



Internal ID20740746
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:90296181..90296755hg38UCSC Ensembl
chr8:91308409..91308983hg19UCSC Ensembl
Cytoband8q21.3
Allele length
AssemblyAllele length
hg38575
hg19575
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6417253
Supporting Variants
Samples
Known GenesLINC00534
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18173706
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00032


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