A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16274143



Internal ID20483361
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:113668963..113669031hg38UCSC Ensembl
chr9:116431243..116431311hg19UCSC Ensembl
Cytoband9q32
Allele length
AssemblyAllele length
hg3869
hg1969
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4743919
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16274143
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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