A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6451704



Internal ID21109257
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:133388956..133400469hg38UCSC Ensembl
chr9:136254740..136265597hg19UCSC Ensembl
Cytoband9q34.2
Allele length
AssemblyAllele length
hg3811514
hg1910858
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18177108
Samples
Known GenesC9orf96
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6451704
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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