A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17356711



Internal ID22582380
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:111558521..111558521hg38UCSC Ensembl
chr11:111429246..111429246hg19UCSC Ensembl
Cytoband11q23.1
Allele length
AssemblyAllele length
hg38456
hg19456
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5977874
Supporting Variants
Samples
Known GenesLAYN
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17356711
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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