A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17688367



Internal ID112033
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:39960742..39967283hg38UCSC Ensembl
chr11:39982292..39988833hg19UCSC Ensembl
Cytoband11p12
Allele length
AssemblyAllele length
hg386542
hg196542
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5498224
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17688367
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000156


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