A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6064633



Internal ID21973866
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:25570018..25570018hg38UCSC Ensembl
chr7:25609638..25609638hg19UCSC Ensembl
Cytoband7p15.2
Allele length
AssemblyAllele length
hg38286
hg19286
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17558620
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6064633
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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