A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18182913



Internal ID20749953
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:43165790..43181883hg38UCSC Ensembl
chr10:43661238..43677331hg19UCSC Ensembl
Cytoband10q11.21
Allele length
AssemblyAllele length
hg3816094
hg1916094
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6455403
Supporting Variants
Samples
Known GenesCSGALNACT2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18182913
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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