A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16266603



Internal ID20475821
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:33215591..33215591hg38UCSC Ensembl
chr19:33706497..33706497hg19UCSC Ensembl
Cytoband19q13.11
Allele length
AssemblyAllele length
hg3888
hg1988
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4753228
Supporting Variants
Samples
Known GenesSLC7A10
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16266603
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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