A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6476103



Internal ID21133656
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:77579669..77580324hg38UCSC Ensembl
chr13:78153804..78154459hg19UCSC Ensembl
Cytoband13q22.3
Allele length
AssemblyAllele length
hg38656
hg19656
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18013217
Samples
Known GenesSCEL
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6476103
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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