A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6425452



Internal ID21083005
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:28600671..28807394hg38UCSC Ensembl
chr9:28600669..28807392hg19UCSC Ensembl
Cytoband9p21.1
Allele length
AssemblyAllele length
hg38206724
hg19206724
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7673n223
Supporting Variantsnssv18187057
Samples
Known GenesLINGO2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6425452
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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