A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5873803



Internal ID22648751
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:19740651..19744688hg38UCSC Ensembl
chr1:20067144..20071181hg19UCSC Ensembl
Cytoband1p36.13
Allele length
AssemblyAllele length
hg384038
hg194038
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17354221
Samples
Known GenesTMCO4
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5873803
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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