A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17438223



Internal ID22496093
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:121642905..121643800hg38UCSC Ensembl
chr9:124405184..124406079hg19UCSC Ensembl
Cytoband9q33.2
Allele length
AssemblyAllele length
hg38896
hg19896
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5925929
Supporting Variants
Samples
Known GenesDAB2IP
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17438223
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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