A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6072629



Internal ID21981862
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:16391674..16391674hg38UCSC Ensembl
chr5:16391783..16391783hg19UCSC Ensembl
Cytoband5p15.1
Allele length
AssemblyAllele length
hg38301
hg19301
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17539378
Samples
Known GenesLOC101929505
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6072629
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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