A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5899276



Internal ID22674404
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:143832500..144032739hg38UCSC Ensembl
chr4:144753653..144953892hg19UCSC Ensembl
Cytoband4q31.21
Allele length
AssemblyAllele length
hg38200240
hg19200240
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1596n209
Supporting Variantsnssv17420934
Samples
Known GenesGYPB, GYPE
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5899276
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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