A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6096344



Internal ID22005577
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:100719106..100719106hg38UCSC Ensembl
chr15:101259311..101259311hg19UCSC Ensembl
Cytoband15q26.3
Allele length
AssemblyAllele length
hg38334
hg19334
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17599621
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6096344
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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