A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6366795



Internal ID21024348
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:129723391..129735062hg38UCSC Ensembl
chr3:129442234..129453905hg19UCSC Ensembl
Cytoband3q22.1
Allele length
AssemblyAllele length
hg3811672
hg1911672
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18093232
Samples
Known GenesTMCC1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6366795
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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