A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18190892



Internal ID20757932
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:84669191..84693709hg38UCSC Ensembl
chr10:86428947..86453465hg19UCSC Ensembl
Cytoband10q23.1
Allele length
AssemblyAllele length
hg3824519
hg1924519
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6448042
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18190892
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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