A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6384342



Internal ID21041895
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:41225566..41230223hg38UCSC Ensembl
chr4:41227583..41232240hg19UCSC Ensembl
Cytoband4p13
Allele length
AssemblyAllele length
hg384658
hg194658
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18116351
Samples
Known GenesUCHL1-AS1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6384342
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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