A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17596222



Internal ID21788265
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:89450399..89450399hg38UCSC Ensembl
chr10:91210156..91210156hg19UCSC Ensembl
Cytoband10q23.31
Allele length
AssemblyAllele length
hg38291
hg19291
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6086312
Supporting Variants
Samples
Known GenesSLC16A12
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17596222
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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