A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5940295



Internal ID22715702
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:67472735..67524890hg38UCSC Ensembl
chr13:68046867..68099022hg19UCSC Ensembl
Cytoband13q21.32
Allele length
AssemblyAllele length
hg3852156
hg1952156
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17386128
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5940295
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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