A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17043945



Internal ID97026
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:42251337..42254211hg38UCSC Ensembl
chr11:42272887..42275761hg19UCSC Ensembl
Cytoband11p12
Allele length
AssemblyAllele length
hg382875
hg192875
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5495906
Supporting Variants
Samples
Known GenesLOC100507205
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17043945
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000156


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