A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17624845



Internal ID21816892
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:27887133..27887133hg38UCSC Ensembl
chr17:26214159..26214159hg19UCSC Ensembl
Cytoband17q11.2
Allele length
AssemblyAllele length
hg38620
hg19620
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6095930
Supporting Variants
Samples
Known GenesLYRM9
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17624845
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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