A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6450273



Internal ID21107826
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:124571545..124572061hg38UCSC Ensembl
chr9:127333824..127334340hg19UCSC Ensembl
Cytoband9q33.3
Allele length
AssemblyAllele length
hg38517
hg19517
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18176613
Samples
Known GenesNR6A1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6450273
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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