A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6029347



Internal ID21938690
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:78855812..78866513hg38UCSC Ensembl
chr15:79148154..79158855hg19UCSC Ensembl
Cytoband15q25.1
Allele length
AssemblyAllele length
hg3810702
hg1910702
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17600057
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6029347
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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