A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17367972



Internal ID22593641
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:92229491..92229491hg38UCSC Ensembl
chr11:91962657..91962657hg19UCSC Ensembl
Cytoband11q14.3
Allele length
AssemblyAllele length
hg38146
hg19146
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5979988
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17367972
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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