A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17049787



Internal ID101086
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:88745942..88785660hg38UCSC Ensembl
chr11:88479110..88518828hg19UCSC Ensembl
Cytoband11q14.3
Allele length
AssemblyAllele length
hg3839719
hg1939719
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5500813
Supporting Variants
Samples
Known GenesGRM5
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17049787
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000156


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