A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18177403



Internal ID20744443
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:73573703..73583530hg38UCSC Ensembl
chr10:75333461..75343288hg19UCSC Ensembl
Cytoband10q22.2
Allele length
AssemblyAllele length
hg389828
hg199828
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6447710
Supporting Variants
Samples
Known GenesUSP54
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18177403
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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