A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6323672



Internal ID20856792
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:46680..171611hg38UCSC Ensembl
chr2:46680..171611hg19UCSC Ensembl
Cytoband2p25.3
Allele length
AssemblyAllele length
hg38124932
hg19124932
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18209821
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6323672
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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