A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16267649



Internal ID20476867
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:38808444..38808547hg38UCSC Ensembl
chr19:39299084..39299187hg19UCSC Ensembl
Cytoband19q13.2
Allele length
AssemblyAllele length
hg38104
hg19104
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4746866
Supporting Variants
Samples
Known GenesLGALS4
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16267649
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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