A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6354061



Internal ID21011614
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:142597213..142661131hg38UCSC Ensembl
chr2:143354782..143418700hg19UCSC Ensembl
Cytoband2q22.2
Allele length
AssemblyAllele length
hg3863919
hg1963919
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18207269
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6354061
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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