A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6035418



Internal ID21944761
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:62820711..62820773hg38UCSC Ensembl
chr11:62588183..62588245hg19UCSC Ensembl
Cytoband11q12.3
Allele length
AssemblyAllele length
hg3863
hg1963
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17583730
Samples
Known GenesSTX5
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6035418
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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