A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6491251



Internal ID21148804
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:74175847..74176200hg38UCSC Ensembl
chr13:74749984..74750337hg19UCSC Ensembl
Cytoband13q22.1
Allele length
AssemblyAllele length
hg38354
hg19354
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18012629
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6491251
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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