A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6340868



Internal ID20998421
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:104656201..104662800hg38UCSC Ensembl
chr2:105272659..105279258hg19UCSC Ensembl
Cytoband2q12.1
Allele length
AssemblyAllele length
hg386600
hg196600
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18205806
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6340868
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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