A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5840776



Internal ID22615711
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:126627935..126651915hg38UCSC Ensembl
chr5:125963627..125987607hg19UCSC Ensembl
Cytoband5q23.2
Allele length
AssemblyAllele length
hg3823981
hg1923981
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17494180
Samples
Known GenesC5orf48
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5840776
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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