A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18177056



Internal ID20744096
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:132666701..132668700hg38UCSC Ensembl
chr9:135542088..135544087hg19UCSC Ensembl
Cytoband9q34.13
Allele length
AssemblyAllele length
hg382000
hg192000
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6437511
Supporting Variants
Samples
Known GenesDDX31
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18177056
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00087


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