A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18220983



Internal ID20788023
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:50529530..50566586hg38UCSC Ensembl
chr8:51442090..51479146hg19UCSC Ensembl
Cytoband8q11.21
Allele length
AssemblyAllele length
hg3837057
hg1937057
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6433678
Supporting Variants
Samples
Known GenesSNTG1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18220983
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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