A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6491047



Internal ID21148600
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:60242701..60245800hg38UCSC Ensembl
chr13:60816835..60819934hg19UCSC Ensembl
Cytoband13q21.2
Allele length
AssemblyAllele length
hg383100
hg193100
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1860n223
Supporting Variantsnssv18010564
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6491047
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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