A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16258979



Internal ID20468167
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:129576170..129576233hg38UCSC Ensembl
chr9:132338449..132338512hg19UCSC Ensembl
Cytoband9q34.11
Allele length
AssemblyAllele length
hg3864
hg1964
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4747113
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16258979
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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