A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18231834



Internal ID20798874
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:61433214..61442858hg38UCSC Ensembl
chr8:62345773..62355417hg19UCSC Ensembl
Cytoband8q12.3
Allele length
AssemblyAllele length
hg389645
hg199645
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6421007
Supporting Variants
Samples
Known GenesCLVS1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18231834
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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