A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18149887



Internal ID20716927
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:114634816..114635339hg38UCSC Ensembl
chr7:114274871..114275394hg19UCSC Ensembl
Cytoband7q31.1
Allele length
AssemblyAllele length
hg38524
hg19524
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6604407
Supporting Variants
Samples
Known GenesFOXP2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18149887
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00024


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