A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18168849



Internal ID20735889
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:36950021..36950351hg38UCSC Ensembl
chr8:36807539..36807869hg19UCSC Ensembl
Cytoband8p11.23
Allele length
AssemblyAllele length
hg38331
hg19331
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6431883
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18168849
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00163


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