A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18193652



Internal ID20760692
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:47182524..47272628hg38UCSC Ensembl
chr10:48466734..48556838hg19UCSC Ensembl
Cytoband10q11.22
Allele length
AssemblyAllele length
hg3890105
hg1990105
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6452677
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18193652
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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