A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6072945



Internal ID21982178
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:17171601..17171601hg38UCSC Ensembl
chr5:17171710..17171710hg19UCSC Ensembl
Cytoband5p15.1
Allele length
AssemblyAllele length
hg3855
hg1955
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17556738
Samples
Known GenesLOC285696
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6072945
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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