A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6388025



Internal ID21045578
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:138822948..138823480hg38UCSC Ensembl
chr4:139744102..139744634hg19UCSC Ensembl
Cytoband4q31.1
Allele length
AssemblyAllele length
hg38533
hg19533
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18110143
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6388025
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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