A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18149888



Internal ID20716928
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:114637465..114637948hg38UCSC Ensembl
chr7:114277520..114278003hg19UCSC Ensembl
Cytoband7q31.1
Allele length
AssemblyAllele length
hg38484
hg19484
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6609450
Supporting Variants
Samples
Known GenesFOXP2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18149888
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.0006


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