A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6038136



Internal ID21947479
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:63048..63139hg38UCSC Ensembl
chr11:128733..128824hg19UCSC Ensembl
Cytoband11p15.5
Allele length
AssemblyAllele length
hg3892
hg1992
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17626920
Samples
Known GenesLINC01001
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6038136
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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