A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6032771



Internal ID21942114
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:128571472..128571523hg38UCSC Ensembl
chr11:128441367..128441418hg19UCSC Ensembl
Cytoband11q24.3
Allele length
AssemblyAllele length
hg3852
hg1952
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17607052
Samples
Known GenesETS1
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6032771
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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