A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv37n223



Internal ID22803005
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:6234901..6236400hg38UCSC Ensembl
chr1:6294961..6296460hg19UCSC Ensembl
Cytoband1p36.31
Allele length
AssemblyAllele length
hg381500
hg191500
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv6335253, nsv6332285
Samples
Known GenesICMT, LINC00337
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)dgv37n223
Frequency
Sample Size19652
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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