A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6343353



Internal ID21000906
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:15325992..15404294hg38UCSC Ensembl
chr2:15466116..15544418hg19UCSC Ensembl
Cytoband2p24.3
Allele length
AssemblyAllele length
hg3878303
hg1978303
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18205552
Samples
Known GenesNBAS
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6343353
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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