A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6096938



Internal ID22006171
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:63982821..63982821hg38UCSC Ensembl
chr15:64275020..64275020hg19UCSC Ensembl
Cytoband15q22.31
Allele length
AssemblyAllele length
hg38113
hg19113
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17615297
Samples
Known GenesDAPK2
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6096938
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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