A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16274201



Internal ID20483419
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:30387376..30387456hg38UCSC Ensembl
chr16:30398697..30398777hg19UCSC Ensembl
Cytoband16p11.2
Allele length
AssemblyAllele length
hg3881
hg1981
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4730876
Supporting Variants
Samples
Known GenesZNF48
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16274201
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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