A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6342534



Internal ID21000087
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:180356968..180367516hg38UCSC Ensembl
chr2:181221695..181232243hg19UCSC Ensembl
Cytoband2q31.3
Allele length
AssemblyAllele length
hg3810549
hg1910549
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18205303
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6342534
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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