A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18195447



Internal ID20762487
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:81500001..81506400hg38UCSC Ensembl
chr10:83259757..83266156hg19UCSC Ensembl
Cytoband10q23.1
Allele length
AssemblyAllele length
hg386400
hg196400
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6435784
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18195447
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.00031


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