A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5843111



Internal ID22618046
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:60884261..60885710hg38UCSC Ensembl
chr5:60180088..60181537hg19UCSC Ensembl
Cytoband5q12.1
Allele length
AssemblyAllele length
hg381450
hg191450
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17499878, nssv17497988
Samples
Known GenesERCC8
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5843111
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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