A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17987478



Internal ID20554520
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:128471165..128471822hg38UCSC Ensembl
chr11:128341060..128341717hg19UCSC Ensembl
Cytoband11q24.3
Allele length
AssemblyAllele length
hg38658
hg19658
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6467610
Supporting Variants
Samples
Known GenesETS1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv17987478
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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