A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5938726



Internal ID22714111
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:70494857..70514667hg38UCSC Ensembl
chr13:71068989..71088799hg19UCSC Ensembl
Cytoband13q21.33
Allele length
AssemblyAllele length
hg3819811
hg1919811
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17380318
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5938726
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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