A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5853928



Internal ID22628863
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:26096400..26107117hg38UCSC Ensembl
chr13:26670538..26681255hg19UCSC Ensembl
Cytoband13q12.13
Allele length
AssemblyAllele length
hg3810718
hg1910718
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17454449
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5853928
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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