A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6366721



Internal ID21024274
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:52890669..52894805hg38UCSC Ensembl
chr3:52924685..52928821hg19UCSC Ensembl
Cytoband3p21.1
Allele length
AssemblyAllele length
hg384137
hg194137
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18100982
Samples
Known GenesTMEM110, TMEM110-MUSTN1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6366721
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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