A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6479602



Internal ID21137155
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:29156947..29157342hg38UCSC Ensembl
chr13:29731084..29731479hg19UCSC Ensembl
Cytoband13q12.3
Allele length
AssemblyAllele length
hg38396
hg19396
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18007848
Samples
Known GenesMTUS2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6479602
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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