A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18169974



Internal ID20737014
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:58495201..58496400hg38UCSC Ensembl
chr8:59407760..59408959hg19UCSC Ensembl
Cytoband8q12.1
Allele length
AssemblyAllele length
hg381200
hg191200
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6417547
Supporting Variants
Samples
Known GenesCYP7A1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18169974
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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