A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17607094



Internal ID21799141
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:70889582..70889582hg38UCSC Ensembl
chr15:71181921..71181921hg19UCSC Ensembl
Cytoband15q23
Allele length
AssemblyAllele length
hg3859
hg1959
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6096695
Supporting Variants
Samples
Known GenesLRRC49, THAP10
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17607094
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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