A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6606405



Internal ID20979476
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:28260894..28269748hg38UCSC Ensembl
chr7:28300513..28309367hg19UCSC Ensembl
Cytoband7p15.1
Allele length
AssemblyAllele length
hg388855
hg198855
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18224846
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6606405
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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