A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14437714



Internal ID22180797
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:155367172..155367250hg38UCSC Ensembl
chr7:155159867..155159945hg19UCSC Ensembl
Cytoband7q36.3
Allele length
AssemblyAllele length
hg3879
hg1979
Variant TypeCNV sva deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3278563
Supporting Variants
SamplesHG00514
Known GenesBLACE
MethodMerging
AnalysisPhasedSV,MsPAC, Multiple Illumina callers, BioNano Genomics software
PlatformSee merged experiments
CommentsAbsence of a SVA mobile element insertion that is present in the reference
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14437714
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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