A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18178043



Internal ID20745083
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:22002301..22004300hg38UCSC Ensembl
chr10:22291230..22293229hg19UCSC Ensembl
Cytoband10p12.31
Allele length
AssemblyAllele length
hg382000
hg192000
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6440550
Supporting Variants
Samples
Known GenesDNAJC1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18178043
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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