A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17073532



Internal ID21437694
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:130532466..130532556hg38UCSC Ensembl
chr11:130402361..130402451hg19UCSC Ensembl
Cytoband11q24.3
Allele length
AssemblyAllele length
hg3891
hg1991
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5598996
Supporting Variants
SamplesHG00731
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17073532
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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