A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17587678



Internal ID21779721
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:64702070..64702244hg38UCSC Ensembl
chr11:64469542..64469716hg19UCSC Ensembl
Cytoband11q13.1
Allele length
AssemblyAllele length
hg38175
hg19175
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6027324
Supporting Variants
Samples
Known GenesNRXN2
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17587678
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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