A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17076878



Internal ID21408959
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:95747274..95747364hg38UCSC Ensembl
chr11:95480438..95480528hg19UCSC Ensembl
Cytoband11q21
Allele length
AssemblyAllele length
hg3891
hg1991
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5588281
Supporting Variants
SamplesHG00512
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17076878
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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