A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6028912



Internal ID21938255
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:47785838..47786274hg38UCSC Ensembl
chr13:48359973..48360409hg19UCSC Ensembl
Cytoband13q14.2
Allele length
AssemblyAllele length
hg38437
hg19437
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17606531
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6028912
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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