A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6388989



Internal ID21046542
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:62338454..62348326hg38UCSC Ensembl
chr4:63204172..63214044hg19UCSC Ensembl
Cytoband4q13.1
Allele length
AssemblyAllele length
hg389873
hg199873
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18118531
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6388989
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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