A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6346835



Internal ID21004388
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:158849264..158870262hg38UCSC Ensembl
chr2:159705776..159726774hg19UCSC Ensembl
Cytoband2q24.1
Allele length
AssemblyAllele length
hg3820999
hg1920999
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4161n223
Supporting Variantsnssv18205593
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6346835
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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