A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6387425



Internal ID21044978
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:96854890..96855449hg38UCSC Ensembl
chr4:97776041..97776600hg19UCSC Ensembl
Cytoband4q22.3
Allele length
AssemblyAllele length
hg38560
hg19560
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18121435
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6387425
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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