A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6609284



Internal ID20982355
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:49124283..49511788hg38UCSC Ensembl
chr7:49163879..49551384hg19UCSC Ensembl
Cytoband7p12.2
Allele length
AssemblyAllele length
hg38387506
hg19387506
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18217481
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6609284
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