A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4734971



Internal ID20510911
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:12261164..12261444hg38UCSC Ensembl
chr16:12355021..12355301hg19UCSC Ensembl
Cytoband16p13.13
Allele length
AssemblyAllele length
hg38281
hg19281
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16280117
Samples
Known GenesSNX29
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4734971
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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