A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6382274



Internal ID21039827
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:141719701..141722000hg38UCSC Ensembl
chr4:142640854..142643153hg19UCSC Ensembl
Cytoband4q31.21
Allele length
AssemblyAllele length
hg382300
hg192300
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18108760
Samples
Known GenesIL15
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6382274
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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