A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5860550



Internal ID22635485
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:44704813..44710585hg38UCSC Ensembl
chr13:45278949..45284721hg19UCSC Ensembl
Cytoband13q14.12
Allele length
AssemblyAllele length
hg385773
hg195773
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17465648
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5860550
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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