A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6037925



Internal ID21947268
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:12318668..12336229hg38UCSC Ensembl
chr16:12412525..12430086hg19UCSC Ensembl
Cytoband16p13.13
Allele length
AssemblyAllele length
hg3817562
hg1917562
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17599188
Samples
Known GenesSNX29
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6037925
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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