A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17703032



Internal ID126698
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:49208818..49259480hg38UCSC Ensembl
chr15:49501015..49551677hg19UCSC Ensembl
Cytoband15q21.2
Allele length
AssemblyAllele length
hg3850663
hg1950663
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5525023
Supporting Variants
Samples
Known GenesGALK2
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17703032
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000312


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