A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6337558



Internal ID20995111
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:97854986..98071280hg38UCSC Ensembl
chr2:98471449..98687743hg19UCSC Ensembl
Cytoband2q11.2
Allele length
AssemblyAllele length
hg38216295
hg19216295
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18208838
Samples
Known GenesTMEM131
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6337558
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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