A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6380831



Internal ID21038384
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:109980089..109980536hg38UCSC Ensembl
chr4:110901245..110901692hg19UCSC Ensembl
Cytoband4q25
Allele length
AssemblyAllele length
hg38448
hg19448
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18107787
Samples
Known GenesEGF
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6380831
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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