A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6380826



Internal ID21038379
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:142951401..142956300hg38UCSC Ensembl
chr4:143872554..143877453hg19UCSC Ensembl
Cytoband4q31.21
Allele length
AssemblyAllele length
hg384900
hg194900
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18213074
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6380826
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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