A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4759653



Internal ID20535514
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:81704204..81704204hg38UCSC Ensembl
chr16:81737809..81737809hg19UCSC Ensembl
Cytoband16q23.3
Allele length
AssemblyAllele length
hg38289
hg19289
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16286145
Samples
Known GenesCMIP
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4759653
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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