A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4746922



Internal ID20522938
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:27051564..27051664hg38UCSC Ensembl
chr13:27625701..27625801hg19UCSC Ensembl
Cytoband13q12.13
Allele length
AssemblyAllele length
hg38101
hg19101
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16266536
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4746922
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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