A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17622415



Internal ID21814462
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:28692261..28692938hg38UCSC Ensembl
chr17:27019279..27019956hg19UCSC Ensembl
Cytoband17q11.2
Allele length
AssemblyAllele length
hg38678
hg19678
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6023193
Supporting Variants
Samples
Known GenesSUPT6H
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17622415
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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