A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6337878



Internal ID20995431
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:101977766..101978058hg38UCSC Ensembl
chr2:102594228..102594520hg19UCSC Ensembl
Cytoband2q11.2
Allele length
AssemblyAllele length
hg38293
hg19293
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18205775
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6337878
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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