A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6047627



Internal ID21956861
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:2737774..2738503hg38UCSC Ensembl
chr19:2737772..2738501hg19UCSC Ensembl
Cytoband19p13.3
Allele length
AssemblyAllele length
hg38730
hg19730
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17622429
Samples
Known GenesSLC39A3
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6047627
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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