A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6067594



Internal ID21976827
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:156655787..156655787hg38UCSC Ensembl
chr7:156448481..156448481hg19UCSC Ensembl
Cytoband7q36.3
Allele length
AssemblyAllele length
hg38315
hg19315
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17570344
Samples
Known GenesRNF32
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6067594
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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