A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16270122



Internal ID20479340
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:29664304..29664368hg38UCSC Ensembl
chr16:29675625..29675689hg19UCSC Ensembl
Cytoband16p11.2
Allele length
AssemblyAllele length
hg3865
hg1965
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4735027
Supporting Variants
Samples
Known GenesSPN
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16270122
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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