A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6044831



Internal ID21954109
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:3096725..3102387hg38UCSC Ensembl
chr19:3096723..3102385hg19UCSC Ensembl
Cytoband19p13.3
Allele length
AssemblyAllele length
hg385663
hg195663
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17636189
Samples
Known GenesGNA11
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6044831
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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