A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6343940



Internal ID21001493
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:14450164..14468614hg38UCSC Ensembl
chr2:14590288..14608738hg19UCSC Ensembl
Cytoband2p24.3
Allele length
AssemblyAllele length
hg3818451
hg1918451
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18207305
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6343940
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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