A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6494187



Internal ID21151740
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:103175274..103175478hg38UCSC Ensembl
chr13:103827624..103827828hg19UCSC Ensembl
Cytoband13q33.1
Allele length
AssemblyAllele length
hg38205
hg19205
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18005962
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6494187
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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