A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18172834



Internal ID20739874
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:92097071..92104083hg38UCSC Ensembl
chr8:93109299..93116311hg19UCSC Ensembl
Cytoband8q21.3
Allele length
AssemblyAllele length
hg387013
hg197013
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6417690
Supporting Variants
Samples
Known GenesRUNX1T1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18172834
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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