A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6320042



Internal ID20853140
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:219840396..219887850hg38UCSC Ensembl
chr1:220013738..220061192hg19UCSC Ensembl
Cytoband1q41
Allele length
AssemblyAllele length
hg3847455
hg1947455
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18202036
Samples
Known GenesRNU5F-1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6320042
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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