A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18179690



Internal ID20746730
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:29404998..29407636hg38UCSC Ensembl
chr10:29693927..29696565hg19UCSC Ensembl
Cytoband10p11.23
Allele length
AssemblyAllele length
hg382639
hg192639
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6439447
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18179690
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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