A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14385997



Internal ID22300526
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:155406019..155409483hg38UCSC Ensembl
chr7:155198714..155202178hg19UCSC Ensembl
Cytoband7q36.3
Allele length
AssemblyAllele length
hg383465
hg193465
Variant TypeOTHER complex substitution
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3179706
Supporting Variants
SamplesNA19240
Known Genes
MethodMerging
AnalysisPhasedSV,MsPAC, Multiple Illumina callers, BioNano Genomics software
PlatformSee merged experiments
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14385997
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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