A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6048132



Internal ID21957365
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:33102217..33102279hg38UCSC Ensembl
chr19:33593123..33593185hg19UCSC Ensembl
Cytoband19q13.11
Allele length
AssemblyAllele length
hg3863
hg1963
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17633086
Samples
Known GenesGPATCH1
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6048132
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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