A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18166829



Internal ID20733869
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:29885863..29886478hg38UCSC Ensembl
chr8:29743379..29743994hg19UCSC Ensembl
Cytoband8p12
Allele length
AssemblyAllele length
hg38616
hg19616
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6430819
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18166829
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00023


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