A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17046709



Internal ID98955
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:64279903..64280630hg38UCSC Ensembl
chr11:64047375..64048102hg19UCSC Ensembl
Cytoband11q13.1
Allele length
AssemblyAllele length
hg38728
hg19728
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5503594
Supporting Variants
Samples
Known GenesBAD
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17046709
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000156


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