A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6318474



Internal ID20851566
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:232735177..232742237hg38UCSC Ensembl
chr1:232870923..232877983hg19UCSC Ensembl
Cytoband1q42.2
Allele length
AssemblyAllele length
hg387061
hg197061
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18202368
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6318474
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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