A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6386908



Internal ID21044461
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:143219854..143220565hg38UCSC Ensembl
chr4:144141007..144141718hg19UCSC Ensembl
Cytoband4q31.21
Allele length
AssemblyAllele length
hg38712
hg19712
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18111333
Samples
Known GenesUSP38
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6386908
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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