A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17072582



Internal ID21474525
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:121185814..121185814hg38UCSC Ensembl
chr11:121056523..121056523hg19UCSC Ensembl
Cytoband11q23.3
Allele length
AssemblyAllele length
hg38237
hg19237
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5651551
Supporting Variants
SamplesHG03371
Known GenesTECTA
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17072582
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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