A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6609392



Internal ID20982463
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:114103547..114104282hg38UCSC Ensembl
chr7:113743602..113744337hg19UCSC Ensembl
Cytoband7q31.1
Allele length
AssemblyAllele length
hg38736
hg19736
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18153536
Samples
Known GenesFOXP2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6609392
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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