A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6444980



Internal ID21102533
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:125310705..125311008hg38UCSC Ensembl
chr9:128072984..128073287hg19UCSC Ensembl
Cytoband9q33.3
Allele length
AssemblyAllele length
hg38304
hg19304
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18176679
Samples
Known GenesGAPVD1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6444980
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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