A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17041765



Internal ID95549
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:7173091..7175033hg38UCSC Ensembl
chr11:7194322..7196264hg19UCSC Ensembl
Cytoband11p15.4
Allele length
AssemblyAllele length
hg381943
hg191943
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5513779
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17041765
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.001561


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