A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6025758



Internal ID21935101
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:412575..412734hg38UCSC Ensembl
chr11:412575..412734hg19UCSC Ensembl
Cytoband11p15.5
Allele length
AssemblyAllele length
hg38160
hg19160
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17586555
Samples
Known GenesSIGIRR
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6025758
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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