A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17688406



Internal ID112072
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:73238983..73240746hg38UCSC Ensembl
chr11:72950028..72951791hg19UCSC Ensembl
Cytoband11q13.4
Allele length
AssemblyAllele length
hg381764
hg191764
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5501775
Supporting Variants
Samples
Known GenesP2RY2
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17688406
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000156


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