A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6429817



Internal ID21087370
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:27562506..27563142hg38UCSC Ensembl
chr9:27562504..27563140hg19UCSC Ensembl
Cytoband9p21.2
Allele length
AssemblyAllele length
hg38637
hg19637
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18185839
Samples
Known GenesC9orf72
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6429817
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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