A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6079864



Internal ID21989097
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:37910181..37910181hg38UCSC Ensembl
chr7:37949783..37949783hg19UCSC Ensembl
Cytoband7p14.1
Allele length
AssemblyAllele length
hg381088
hg191088
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17572279
Samples
Known GenesSFRP4
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6079864
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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