A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17057017



Internal ID105850
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:29884311..29884739hg38UCSC Ensembl
chr12:30037244..30037672hg19UCSC Ensembl
Cytoband12p11.22
Allele length
AssemblyAllele length
hg38429
hg19429
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5512059
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17057017
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000312


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