A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17367421



Internal ID22593090
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:47299623..47299623hg38UCSC Ensembl
chr11:47321174..47321174hg19UCSC Ensembl
Cytoband11p11.2
Allele length
AssemblyAllele length
hg3853
hg1953
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5978814
Supporting Variants
Samples
Known GenesMADD
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17367421
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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