A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6427327



Internal ID21084880
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:22656617..22743006hg38UCSC Ensembl
chr9:22656616..22743005hg19UCSC Ensembl
Cytoband9p21.3
Allele length
AssemblyAllele length
hg3886390
hg1986390
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18176178
Samples
Known GenesFLJ35282
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6427327
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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