A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17632929



Internal ID21824976
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:53625373..53625547hg38UCSC Ensembl
chr16:53659285..53659459hg19UCSC Ensembl
Cytoband16q12.2
Allele length
AssemblyAllele length
hg38175
hg19175
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6021581
Supporting Variants
Samples
Known GenesRPGRIP1L
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17632929
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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