A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6021466



Internal ID21930809
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:70823138..70823354hg38UCSC Ensembl
chr11:70669243..70669459hg19UCSC Ensembl
Cytoband11q13.4
Allele length
AssemblyAllele length
hg38217
hg19217
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17586293
Samples
Known GenesSHANK2
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6021466
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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