A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18221299



Internal ID20788339
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:8867324..8886761hg38UCSC Ensembl
chr8:8724834..8744271hg19UCSC Ensembl
Cytoband8p23.1
Allele length
AssemblyAllele length
hg3819438
hg1919438
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6426507
Supporting Variants
Samples
Known GenesMFHAS1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18221299
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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