A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6338038



Internal ID20995591
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:179266010..179426259hg38UCSC Ensembl
chr2:180130737..180290986hg19UCSC Ensembl
Cytoband2q31.2
Allele length
AssemblyAllele length
hg38160250
hg19160250
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18204686
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6338038
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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