A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17616911



Internal ID21808958
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:80836618..80836618hg38UCSC Ensembl
chr15:81128959..81128959hg19UCSC Ensembl
Cytoband15q25.1
Allele length
AssemblyAllele length
hg3871
hg1971
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6095795
Supporting Variants
Samples
Known GenesKIAA1199
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17616911
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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