A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6422357



Internal ID21079910
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:28431993..28489496hg38UCSC Ensembl
chr9:28431991..28489494hg19UCSC Ensembl
Cytoband9p21.1
Allele length
AssemblyAllele length
hg3857504
hg1957504
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18232350
Samples
Known GenesLINGO2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6422357
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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