A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6341226



Internal ID20998779
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:158852849..158874010hg38UCSC Ensembl
chr2:159709361..159730522hg19UCSC Ensembl
Cytoband2q24.1
Allele length
AssemblyAllele length
hg3821162
hg1921162
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4161n223
Supporting Variantsnssv18205595
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6341226
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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