A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18190056



Internal ID20757096
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:9257822..9284303hg38UCSC Ensembl
chr10:9299785..9326266hg19UCSC Ensembl
Cytoband10p14
Allele length
AssemblyAllele length
hg3826482
hg1926482
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6442110
Supporting Variants
Samples
Known GenesLINC00709
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18190056
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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