A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5848715



Internal ID22623650
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:98475946..98477798hg38UCSC Ensembl
chr13:99128200..99130052hg19UCSC Ensembl
Cytoband13q32.2
Allele length
AssemblyAllele length
hg381853
hg191853
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv560n209
Supporting Variantsnssv17459711, nssv17464528
Samples
Known GenesSTK24
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5848715
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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