A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17446109



Internal ID22503979
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:113395802..113398525hg38UCSC Ensembl
chr9:116158082..116160805hg19UCSC Ensembl
Cytoband9q32
Allele length
AssemblyAllele length
hg382724
hg192724
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5924836
Supporting Variants
Samples
Known GenesALAD
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17446109
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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