A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6477015



Internal ID21134568
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:63209763..63315214hg38UCSC Ensembl
chr13:63783896..63889347hg19UCSC Ensembl
Cytoband13q21.31
Allele length
AssemblyAllele length
hg38105452
hg19105452
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18011197
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6477015
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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