A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17044639



Internal ID97501
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:32042948..32042981hg38UCSC Ensembl
chr11:32064494..32064527hg19UCSC Ensembl
Cytoband11p13
Allele length
AssemblyAllele length
hg3859
hg1959
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5547578
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17044639
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.000312


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