A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6052035



Internal ID21961268
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:48011371..48011508hg38UCSC Ensembl
chr19:48514628..48514765hg19UCSC Ensembl
Cytoband19q13.33
Allele length
AssemblyAllele length
hg38138
hg19138
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17628908
Samples
Known GenesELSPBP1
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6052035
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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