A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16274689



Internal ID20483907
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:32694029..32694104hg38UCSC Ensembl
chr9:32694027..32694102hg19UCSC Ensembl
Cytoband9p21.1
Allele length
AssemblyAllele length
hg3876
hg1976
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4735618
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16274689
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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