A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18169206



Internal ID20736246
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:56577746..56579445hg38UCSC Ensembl
chr8:57490305..57492004hg19UCSC Ensembl
Cytoband8q12.1
Allele length
AssemblyAllele length
hg381700
hg191700
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6427489
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18169206
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00054


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