A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16295578



Internal ID20504796
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:43643679..43643783hg38UCSC Ensembl
chr19:44147831..44147935hg19UCSC Ensembl
Cytoband19q13.31
Allele length
AssemblyAllele length
hg38105
hg19105
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4734495
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16295578
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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