A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6379639



Internal ID21037192
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:76243936..76246237hg38UCSC Ensembl
chr4:77165089..77167390hg19UCSC Ensembl
Cytoband4q21.1
Allele length
AssemblyAllele length
hg382302
hg192302
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18120254
Samples
Known GenesFAM47E
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6379639
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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