A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17579235



Internal ID21771278
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:121642009..121642069hg38UCSC Ensembl
chr9:124404288..124404348hg19UCSC Ensembl
Cytoband9q33.2
Allele length
AssemblyAllele length
hg3861
hg1961
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6010521
Supporting Variants
Samples
Known GenesDAB2IP
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17579235
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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