A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3179706



Internal ID22335699
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:155406019..155409483hg38UCSC Ensembl
chr7:155198714..155202178hg19UCSC Ensembl
Cytoband7q36.3
Allele length
AssemblyAllele length
hg383465
hg193465
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv8871n152
Supporting Variantsnssv14385997, nssv14388559
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)nsv3179706
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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