A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18189452



Internal ID20756492
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:36659027..36684523hg38UCSC Ensembl
chr10:36947955..36973451hg19UCSC Ensembl
Cytoband10p11.21
Allele length
AssemblyAllele length
hg3825497
hg1925497
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6443925
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18189452
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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