A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6384078



Internal ID21041631
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:41876273..41885035hg38UCSC Ensembl
chr4:41878290..41887052hg19UCSC Ensembl
Cytoband4p13
Allele length
AssemblyAllele length
hg388763
hg198763
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18116388
Samples
Known GenesLINC00682
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6384078
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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