A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6342574



Internal ID21000127
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:41247719..41592180hg38UCSC Ensembl
chr2:41474859..41819320hg19UCSC Ensembl
Cytoband2p21
Allele length
AssemblyAllele length
hg38344462
hg19344462
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18209180
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6342574
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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