A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17446859



Internal ID22504729
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:100156552..100156637hg38UCSC Ensembl
chr9:102918834..102918919hg19UCSC Ensembl
Cytoband9q31.1
Allele length
AssemblyAllele length
hg3886
hg1986
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5910839
Supporting Variants
Samples
Known GenesINVS
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17446859
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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