A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6099814



Internal ID22009047
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:35756807..35756807hg38UCSC Ensembl
chr15:36049008..36049008hg19UCSC Ensembl
Cytoband15q14
Allele length
AssemblyAllele length
hg38320
hg19320
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17608103
Samples
Known GenesDPH6-AS1
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6099814
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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