A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv5738n223



Internal ID22808706
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:43237201..43243000hg38UCSC Ensembl
chr5:43237303..43243102hg19UCSC Ensembl
Cytoband5p12
Allele length
AssemblyAllele length
hg385800
hg195800
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv6395041, nsv6375755
Samples
Known GenesNIM1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)dgv5738n223
Frequency
Sample Size19652
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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