A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5942062



Internal ID22717493
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:76600346..76605819hg38UCSC Ensembl
chr13:77174481..77179954hg19UCSC Ensembl
Cytoband13q22.2
Allele length
AssemblyAllele length
hg385474
hg195474
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17386142
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5942062
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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