A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6370957



Internal ID21028510
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:133344701..133347400hg38UCSC Ensembl
chr3:133063545..133066244hg19UCSC Ensembl
Cytoband3q22.1
Allele length
AssemblyAllele length
hg382700
hg192700
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18094789
Samples
Known GenesTMEM108
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6370957
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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