A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17622211



Internal ID21814258
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:29134926..29135853hg38UCSC Ensembl
chr17:27461944..27462871hg19UCSC Ensembl
Cytoband17q11.2
Allele length
AssemblyAllele length
hg38928
hg19928
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6028172
Supporting Variants
Samples
Known GenesMYO18A
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17622211
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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