A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6100397



Internal ID22009630
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:83271677..83271677hg38UCSC Ensembl
chr15:83940429..83940429hg19UCSC Ensembl
Cytoband15q25.2
Allele length
AssemblyAllele length
hg38310
hg19310
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17604154
Samples
Known GenesBNC1
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6100397
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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