A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6479129



Internal ID21136682
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:102278601..102280100hg38UCSC Ensembl
chr13:102930951..102932450hg19UCSC Ensembl
Cytoband13q33.1
Allele length
AssemblyAllele length
hg381500
hg191500
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18006365
Samples
Known GenesFGF14
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6479129
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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