A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6381797



Internal ID21039350
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:169219387..169221694hg38UCSC Ensembl
chr4:170140538..170142845hg19UCSC Ensembl
Cytoband4q33
Allele length
AssemblyAllele length
hg382308
hg192308
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18115392
Samples
Known GenesSH3RF1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6381797
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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