A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6074406



Internal ID21983639
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:73306874..73306874hg38UCSC Ensembl
chr7:72720870..72720870hg19UCSC Ensembl
Cytoband7q11.23
Allele length
AssemblyAllele length
hg3895
hg1995
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17566697
Samples
Known GenesNSUN5
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6074406
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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