A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5842124



Internal ID22617059
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:172066466..172068027hg38UCSC Ensembl
chr5:171493470..171495031hg19UCSC Ensembl
Cytoband5q35.1
Allele length
AssemblyAllele length
hg381562
hg191562
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17497701
Samples
Known GenesSTK10
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5842124
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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