A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6616542



Internal ID20989613
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:98547995..98548576hg38UCSC Ensembl
chr7:98177307..98177888hg19UCSC Ensembl
Cytoband7q22.1
Allele length
AssemblyAllele length
hg38582
hg19582
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18225517
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6616542
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer