A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6077670



Internal ID21986903
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:95876042..95876042hg38UCSC Ensembl
chr7:95505354..95505354hg19UCSC Ensembl
Cytoband7q21.3
Allele length
AssemblyAllele length
hg3875
hg1975
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17563831
Samples
Known GenesDYNC1I1
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6077670
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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