A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16286342



Internal ID20495560
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:121649213..121649514hg38UCSC Ensembl
chr9:124411492..124411793hg19UCSC Ensembl
Cytoband9q33.2
Allele length
AssemblyAllele length
hg38302
hg19302
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4731011
Supporting Variants
Samples
Known GenesDAB2IP
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16286342
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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