A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4767292



Internal ID20543152
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:14532398..14532398hg38UCSC Ensembl
chr16:14626255..14626255hg19UCSC Ensembl
Cytoband16p13.12
Allele length
AssemblyAllele length
hg38505
hg19505
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16286226
Samples
Known GenesPARN
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4767292
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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