A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6025656



Internal ID21934999
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:128531..128679hg38UCSC Ensembl
chr11:128531..128679hg19UCSC Ensembl
Cytoband11p15.5
Allele length
AssemblyAllele length
hg38149
hg19149
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17588058
Samples
Known GenesLINC01001
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6025656
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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