A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5937894



Internal ID22713268
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:60817556..60817689hg38UCSC Ensembl
chr13:61391690..61391823hg19UCSC Ensembl
Cytoband13q21.2
Allele length
AssemblyAllele length
hg38134
hg19134
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17374518
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5937894
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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