A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18228648



Internal ID20795688
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:37298859..37299285hg38UCSC Ensembl
chr6:37266635..37267061hg19UCSC Ensembl
Cytoband6p21.2
Allele length
AssemblyAllele length
hg38427
hg19427
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6396352
Supporting Variants
Samples
Known GenesTBC1D22B
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18228648
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.00098


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