A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6049344



Internal ID21958578
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:3096301..3096357hg38UCSC Ensembl
chr19:3096299..3096355hg19UCSC Ensembl
Cytoband19p13.3
Allele length
AssemblyAllele length
hg3857
hg1957
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17632177
Samples
Known GenesGNA11
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6049344
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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