A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17045995



Internal ID98454
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:30103002..30110322hg38UCSC Ensembl
chr11:30124549..30131869hg19UCSC Ensembl
Cytoband11p14.1
Allele length
AssemblyAllele length
hg387321
hg197321
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5504090
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17045995
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000312


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