A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5853069



Internal ID22628004
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:44243692..44245665hg38UCSC Ensembl
chr13:44817828..44819801hg19UCSC Ensembl
Cytoband13q14.11
Allele length
AssemblyAllele length
hg381974
hg191974
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17451971
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5853069
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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