A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17635751



Internal ID21827798
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:52558276..52558276hg38UCSC Ensembl
chr16:52592188..52592188hg19UCSC Ensembl
Cytoband16q12.1
Allele length
AssemblyAllele length
hg38199
hg19199
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6095977
Supporting Variants
Samples
Known GenesCASC16
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17635751
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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