A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6052475



Internal ID21961708
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:49437819..49438019hg38UCSC Ensembl
chr19:49941076..49941276hg19UCSC Ensembl
Cytoband19q13.33
Allele length
AssemblyAllele length
hg38201
hg19201
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17628396
Samples
Known GenesSLC17A7
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6052475
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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