A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6342030



Internal ID20999583
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:5195805..5209592hg38UCSC Ensembl
chr2:5335938..5349725hg19UCSC Ensembl
Cytoband2p25.2
Allele length
AssemblyAllele length
hg3813788
hg1913788
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18209884
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6342030
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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