A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18196971



Internal ID20764011
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:130234456..130239033hg38UCSC Ensembl
chr10:132032720..132037297hg19UCSC Ensembl
Cytoband10q26.3
Allele length
AssemblyAllele length
hg384578
hg194578
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6455275
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18196971
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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