A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18186636



Internal ID20753676
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:28127106..28127899hg38UCSC Ensembl
chr9:28127104..28127897hg19UCSC Ensembl
Cytoband9p21.1
Allele length
AssemblyAllele length
hg38794
hg19794
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6423120
Supporting Variants
Samples
Known GenesLINGO2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18186636
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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