A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6485480



Internal ID21143033
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:72708501..72709800hg38UCSC Ensembl
chr13:73282639..73283938hg19UCSC Ensembl
Cytoband13q21.33
Allele length
AssemblyAllele length
hg381300
hg191300
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18012801
Samples
Known GenesMZT1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6485480
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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