A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6026042



Internal ID21935385
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:70823190..70823250hg38UCSC Ensembl
chr11:70669295..70669355hg19UCSC Ensembl
Cytoband11q13.4
Allele length
AssemblyAllele length
hg3861
hg1961
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17596965
Samples
Known GenesSHANK2
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6026042
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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