A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5843413



Internal ID22618348
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:73787002..73790685hg38UCSC Ensembl
chr5:73082827..73086510hg19UCSC Ensembl
Cytoband5q13.2
Allele length
AssemblyAllele length
hg383684
hg193684
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17498142
Samples
Known GenesARHGEF28
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5843413
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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