A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6445237



Internal ID21102790
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:120673680..120681065hg38UCSC Ensembl
chr9:123435958..123443343hg19UCSC Ensembl
Cytoband9q33.2
Allele length
AssemblyAllele length
hg387386
hg197386
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18174048
Samples
Known GenesMEGF9
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6445237
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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