A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5839496



Internal ID22614431
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:83598600..83600235hg38UCSC Ensembl
chr4:84519753..84521388hg19UCSC Ensembl
Cytoband4q21.23
Allele length
AssemblyAllele length
hg381636
hg191636
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17497842
Samples
Known GenesAGPAT9
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5839496
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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