A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5871939



Internal ID22646877
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:19778087..19778870hg38UCSC Ensembl
chr1:20104580..20105363hg19UCSC Ensembl
Cytoband1p36.13
Allele length
AssemblyAllele length
hg38784
hg19784
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17351688
Samples
Known GenesTMCO4
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5871939
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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