A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6035172



Internal ID21944515
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:128584976..128585076hg38UCSC Ensembl
chr11:128454871..128454971hg19UCSC Ensembl
Cytoband11q24.3
Allele length
AssemblyAllele length
hg38101
hg19101
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17597684
Samples
Known GenesETS1
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6035172
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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