A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17044631



Internal ID97496
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:31964526..31970217hg38UCSC Ensembl
chr11:31986072..31991763hg19UCSC Ensembl
Cytoband11p13
Allele length
AssemblyAllele length
hg385692
hg195692
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5496720
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17044631
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000156


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