A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5840677



Internal ID22615612
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:113298168..113300266hg38UCSC Ensembl
chr5:112633865..112635963hg19UCSC Ensembl
Cytoband5q22.2
Allele length
AssemblyAllele length
hg382099
hg192099
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1706n209
Supporting Variantsnssv17493113, nssv17493112
Samples
Known GenesMCC
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5840677
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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