A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17056566



Internal ID105534
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:55214128..55226200hg38UCSC Ensembl
chr12:55607912..55619984hg19UCSC Ensembl
Cytoband12q13.2
Allele length
AssemblyAllele length
hg3812073
hg1912073
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5513557
Supporting Variants
Samples
Known GenesOR10A7
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17056566
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000157


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