A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6451025



Internal ID21108578
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:90578628..90580028hg38UCSC Ensembl
chr9:93340910..93342310hg19UCSC Ensembl
Cytoband9q22.2
Allele length
AssemblyAllele length
hg381401
hg191401
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18195007
Samples
Known GenesLOC340515
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6451025
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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