A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17437924



Internal ID22495794
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:128198764..128201404hg38UCSC Ensembl
chr9:130961043..130963683hg19UCSC Ensembl
Cytoband9q34.11
Allele length
AssemblyAllele length
hg382641
hg192641
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5925230
Supporting Variants
Samples
Known GenesCIZ1
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17437924
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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