A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6384117



Internal ID21041670
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:112465349..112471043hg38UCSC Ensembl
chr4:113386505..113392199hg19UCSC Ensembl
Cytoband4q25
Allele length
AssemblyAllele length
hg385695
hg195695
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18105626
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6384117
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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