A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17072477



Internal ID21486278
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:1078921..1078921hg38UCSC Ensembl
chr11:1078994..1078994hg19UCSC Ensembl
Cytoband11p15.5
Allele length
AssemblyAllele length
hg381000
hg191000
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5650279
Supporting Variants
SamplesNA12878
Known GenesMUC2
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17072477
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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