A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6606450



Internal ID20979521
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:98445508..98459595hg38UCSC Ensembl
chr7:98074820..98088907hg19UCSC Ensembl
Cytoband7q22.1
Allele length
AssemblyAllele length
hg3814088
hg1914088
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18219253
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6606450
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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