A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv4n223



Internal ID22802972
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:785093..922257hg38UCSC Ensembl
chr1:720473..857637hg19UCSC Ensembl
Cytoband1p36.33
Allele length
AssemblyAllele length
hg38137165
hg19137165
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv6332337, nsv6325716
Samples
Known GenesFAM41C, FAM87B, LINC00115, LINC01128, LOC100130417
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)dgv4n223
Frequency
Sample Size19652
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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