A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5533876



Internal ID309753
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:72954287..72955499hg38UCSC Ensembl
chr17:70950426..70951638hg19UCSC Ensembl
Cytoband17q25.1
Allele length
AssemblyAllele length
hg381213
hg191213
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17714461
Samples
Known GenesSLC39A11
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5533876
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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