A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16283679



Internal ID20492897
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:51357363..51357363hg38UCSC Ensembl
chr19:51860617..51860617hg19UCSC Ensembl
Cytoband19q13.41
Allele length
AssemblyAllele length
hg38320
hg19320
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4760621
Supporting Variants
Samples
Known GenesETFB
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16283679
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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