A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv4139n223



Internal ID22807107
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:141407814..141520856hg38UCSC Ensembl
chr2:142165383..142278425hg19UCSC Ensembl
Cytoband2q22.1
Allele length
AssemblyAllele length
hg38113043
hg19113043
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv6340659, nsv6338275
Samples
Known GenesLRP1B
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)dgv4139n223
Frequency
Sample Size19652
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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