A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6449924



Internal ID21107477
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:119332918..119382264hg38UCSC Ensembl
chr9:122095196..122144542hg19UCSC Ensembl
Cytoband9q33.1
Allele length
AssemblyAllele length
hg3849347
hg1949347
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18225330
Samples
Known GenesBRINP1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6449924
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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