A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5851007



Internal ID22625942
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:49314348..49317297hg38UCSC Ensembl
chr13:49888484..49891433hg19UCSC Ensembl
Cytoband13q14.2
Allele length
AssemblyAllele length
hg382950
hg192950
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17454641
Samples
Known GenesCAB39L
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5851007
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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