A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5927854



Internal ID22703086
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:52783764..52789150hg38UCSC Ensembl
chr13:53357899..53363285hg19UCSC Ensembl
Cytoband13q14.3
Allele length
AssemblyAllele length
hg385387
hg195387
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17381582
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5927854
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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