A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5931604



Internal ID22706891
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:110827162..110827260hg38UCSC Ensembl
chr13:111479509..111479607hg19UCSC Ensembl
Cytoband13q34
Allele length
AssemblyAllele length
hg3899
hg1999
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17362321
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5931604
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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