A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17046745



Internal ID98977
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:64702500..64713074hg38UCSC Ensembl
chr11:64469972..64480546hg19UCSC Ensembl
Cytoband11q13.1
Allele length
AssemblyAllele length
hg3810575
hg1910575
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5494901
Supporting Variants
Samples
Known GenesNRXN2
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17046745
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000156


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