A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18165385



Internal ID20732426
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:19926170..19962499hg38UCSC Ensembl
chr8:19783681..19820010hg19UCSC Ensembl
Cytoband8p21.3
Allele length
AssemblyAllele length
hg3836330
hg1936330
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6424355
Supporting Variants
Samples
Known GenesLPL
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18165385
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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