A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14437859



Internal ID22180951
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:419392..420103hg38UCSC Ensembl
chr7:459358..460069hg19UCSC Ensembl
Cytoband7p22.3
Allele length
AssemblyAllele length
hg38712
hg19712
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3201338
Supporting Variants
SamplesHG00514
Known Genes
MethodMerging
AnalysisPhasedSV,MsPAC, Multiple Illumina callers, BioNano Genomics software
PlatformSee merged experiments
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14437859
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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