A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18192689



Internal ID20759729
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:57713367..57743285hg38UCSC Ensembl
chr10:59473127..59503045hg19UCSC Ensembl
Cytoband10q21.1
Allele length
AssemblyAllele length
hg3829919
hg1929919
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6437601
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18192689
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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