A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17041441



Internal ID95333
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:15062471..15063111hg38UCSC Ensembl
chr11:15084017..15084657hg19UCSC Ensembl
Cytoband11p15.2
Allele length
AssemblyAllele length
hg38641
hg19641
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6143651
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17041441
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.141705


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