A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5842273



Internal ID22617208
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:1880421..1881678hg38UCSC Ensembl
chr5:1880535..1881792hg19UCSC Ensembl
Cytoband5p15.33
Allele length
AssemblyAllele length
hg381258
hg191258
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17495094, nssv17495093
Samples
Known GenesIRX4
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5842273
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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