A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17685107



Internal ID108773
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:124791568..124793693hg38UCSC Ensembl
chr12:125276114..125278239hg19UCSC Ensembl
Cytoband12q24.31
Allele length
AssemblyAllele length
hg382126
hg192126
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5506656
Supporting Variants
Samples
Known GenesSCARB1
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17685107
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00172


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