A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17361529



Internal ID22587198
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:47782304..47782304hg38UCSC Ensembl
chr11:47803856..47803856hg19UCSC Ensembl
Cytoband11p11.2
Allele length
AssemblyAllele length
hg38161
hg19161
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5974441
Supporting Variants
Samples
Known GenesNUP160
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17361529
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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