A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17054101



Internal ID103896
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:24269641..24269909hg38UCSC Ensembl
chr12:24422575..24422843hg19UCSC Ensembl
Cytoband12p12.1
Allele length
AssemblyAllele length
hg38269
hg19269
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5512505
Supporting Variants
Samples
Known GenesSOX5
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17054101
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000937


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