A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17046665



Internal ID98924
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:63854600..63855199hg38UCSC Ensembl
chr11:63622072..63622671hg19UCSC Ensembl
Cytoband11q13.1
Allele length
AssemblyAllele length
hg38600
hg19600
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5507993
Supporting Variants
Samples
Known GenesMARK2
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17046665
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.001873


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