A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17434599



Internal ID22492469
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:104132666..104133854hg38UCSC Ensembl
chr9:106894947..106896135hg19UCSC Ensembl
Cytoband9q31.1
Allele length
AssemblyAllele length
hg381189
hg191189
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5921196
Supporting Variants
Samples
Known GenesSMC2
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17434599
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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