A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6371831



Internal ID21029384
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:31283601..31300100hg38UCSC Ensembl
chr4:31285223..31301722hg19UCSC Ensembl
Cytoband4p15.1
Allele length
AssemblyAllele length
hg3816500
hg1916500
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18114825
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6371831
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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