A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6070514



Internal ID21979747
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:93728065..93728065hg38UCSC Ensembl
chr7:93357377..93357377hg19UCSC Ensembl
Cytoband7q21.3
Allele length
AssemblyAllele length
hg38315
hg19315
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17565172
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6070514
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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