A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5850102



Internal ID22625037
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:114270251..114272912hg38UCSC Ensembl
chr13:115035726..115038387hg19UCSC Ensembl
Cytoband13q34
Allele length
AssemblyAllele length
hg382662
hg192662
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17456195
Samples
Known GenesCDC16
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5850102
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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