A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6030645



Internal ID21939988
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:15080879..15080955hg38UCSC Ensembl
chr16:15174736..15174812hg19UCSC Ensembl
Cytoband16p13.11
Allele length
AssemblyAllele length
hg3877
hg1977
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17612263
Samples
Known GenesPDXDC1, RRN3
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6030645
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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