A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17618441



Internal ID21810488
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:75575115..75580661hg38UCSC Ensembl
chr17:73571196..73576742hg19UCSC Ensembl
Cytoband17q25.1
Allele length
AssemblyAllele length
hg385547
hg195547
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6030152
Supporting Variants
Samples
Known GenesLLGL2
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17618441
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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