A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5928648



Internal ID22703891
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:26196510..26199244hg38UCSC Ensembl
chr13:26770647..26773381hg19UCSC Ensembl
Cytoband13q12.13
Allele length
AssemblyAllele length
hg382735
hg192735
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17388230
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5928648
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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