A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5843586



Internal ID22618521
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:94515829..94517183hg38UCSC Ensembl
chr5:93851534..93852888hg19UCSC Ensembl
Cytoband5q15
Allele length
AssemblyAllele length
hg381355
hg191355
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17500440
Samples
Known GenesKIAA0825
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5843586
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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