A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6031400



Internal ID21940743
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:63922424..64000415hg38UCSC Ensembl
chr15:64214623..64292614hg19UCSC Ensembl
Cytoband15q22.31
Allele length
AssemblyAllele length
hg3877992
hg1977992
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17600661
Samples
Known GenesDAPK2
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6031400
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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