A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6334177



Internal ID20867359
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:218690357..218691759hg38UCSC Ensembl
chr1:218863699..218865101hg19UCSC Ensembl
Cytoband1q41
Allele length
AssemblyAllele length
hg381403
hg191403
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18200600
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6334177
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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