A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17073523



Internal ID21487678
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:130294410..130294410hg38UCSC Ensembl
chr11:130164305..130164305hg19UCSC Ensembl
Cytoband11q24.3
Allele length
AssemblyAllele length
hg382635
hg192635
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5654175
Supporting Variants
SamplesNA18534
Known GenesZBTB44
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17073523
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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