A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18184421



Internal ID20751461
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:130983001..131185100hg38UCSC Ensembl
chr10:132781264..132983363hg19UCSC Ensembl
Cytoband10q26.3
Allele length
AssemblyAllele length
hg38202100
hg19202100
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6439552
Supporting Variants
Samples
Known GenesTCERG1L
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18184421
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.00032


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