A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6339485



Internal ID20997038
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:4194530..4231321hg38UCSC Ensembl
chr2:4242120..4278911hg19UCSC Ensembl
Cytoband2p25.3
Allele length
AssemblyAllele length
hg3836792
hg1936792
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18209764
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6339485
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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