A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6078108



Internal ID21987341
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:70816989..70816989hg38UCSC Ensembl
chr4:71682706..71682706hg19UCSC Ensembl
Cytoband4q13.3
Allele length
AssemblyAllele length
hg38314
hg19314
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17544121
Samples
Known GenesGRSF1
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6078108
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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