A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18173586



Internal ID20740626
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:98912531..98917455hg38UCSC Ensembl
chr8:99924759..99929683hg19UCSC Ensembl
Cytoband8q22.2
Allele length
AssemblyAllele length
hg384925
hg194925
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6420175
Supporting Variants
Samples
Known GenesSTK3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18173586
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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