A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6363472



Internal ID21021025
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:167741348..167747528hg38UCSC Ensembl
chr3:167459136..167465316hg19UCSC Ensembl
Cytoband3q26.1
Allele length
AssemblyAllele length
hg386181
hg196181
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18208589
Samples
Known GenesSERPINI1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6363472
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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