A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6381517



Internal ID21039070
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:70001024..70001326hg38UCSC Ensembl
chr4:70866741..70867043hg19UCSC Ensembl
Cytoband4q13.3
Allele length
AssemblyAllele length
hg38303
hg19303
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18211706
Samples
Known GenesSTATH
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6381517
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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