A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18181208



Internal ID20748248
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:130996301..131179500hg38UCSC Ensembl
chr10:132794564..132977763hg19UCSC Ensembl
Cytoband10q26.3
Allele length
AssemblyAllele length
hg38183200
hg19183200
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6439408
Supporting Variants
Samples
Known GenesTCERG1L
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18181208
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.00023


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