A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17607052



Internal ID21799099
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 StatusS
Merged Variantsnsv6032771
Supporting Variants
Samples
Known GenesETS1
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17607052
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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