A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6360541



Internal ID21018094
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:129894795..129895122hg38UCSC Ensembl
chr3:129613638..129613965hg19UCSC Ensembl
Cytoband3q22.1
Allele length
AssemblyAllele length
hg38328
hg19328
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18093246
Samples
Known GenesTMCC1-AS1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6360541
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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