A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6422512



Internal ID21080065
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:27283380..28841224hg38UCSC Ensembl
chr9:27283378..28841222hg19UCSC Ensembl
Cytoband9p21.1
Allele length
AssemblyAllele length
hg381557845
hg191557845
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18196366
Samples
Known GenesC9orf72, EQTN, IFNK, LINGO2, MOB3B
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6422512
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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