A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5849979



Internal ID22624914
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:93163062..93167943hg38UCSC Ensembl
chr13:93815315..93820196hg19UCSC Ensembl
Cytoband13q31.3
Allele length
AssemblyAllele length
hg384882
hg194882
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17468368
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5849979
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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