A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5891801



Internal ID22666843
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:103093568..103093651hg38UCSC Ensembl
chr4:104014725..104014808hg19UCSC Ensembl
Cytoband4q24
Allele length
AssemblyAllele length
hg3884
hg1984
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17425066
Samples
Known GenesBDH2
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5891801
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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