A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5902326



Internal ID22677483
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:41124501..41124558hg38UCSC Ensembl
chr4:41126518..41126575hg19UCSC Ensembl
Cytoband4p14
Allele length
AssemblyAllele length
hg3858
hg1958
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17423828
Samples
Known GenesAPBB2
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5902326
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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