A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6072474



Internal ID21981707
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:137946946..137946946hg38UCSC Ensembl
chr7:137631692..137631692hg19UCSC Ensembl
Cytoband7q33
Allele length
AssemblyAllele length
hg38261
hg19261
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17560536
Samples
Known GenesCREB3L2
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6072474
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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