A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6384098



Internal ID21041651
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:108458740..108459163hg38UCSC Ensembl
chr4:109379896..109380319hg19UCSC Ensembl
Cytoband4q25
Allele length
AssemblyAllele length
hg38424
hg19424
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18107687
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6384098
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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