A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6353718



Internal ID21011271
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:128074721..128088040hg38UCSC Ensembl
chr2:128832295..128845614hg19UCSC Ensembl
Cytoband2q14.3
Allele length
AssemblyAllele length
hg3813320
hg1913320
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18208225
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6353718
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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