A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5894064



Internal ID22669133
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:121361094..121368795hg38UCSC Ensembl
chr4:122282249..122289950hg19UCSC Ensembl
Cytoband4q27
Allele length
AssemblyAllele length
hg387702
hg197702
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17425130
Samples
Known GenesQRFPR
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5894064
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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