A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3183514



Internal ID22337657
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:155207024..155209961hg38UCSC Ensembl
chr7:154998734..155001671hg19UCSC Ensembl
Cytoband7q36.2
Allele length
AssemblyAllele length
hg382938
hg192938
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14457516, nssv14456633
SamplesHG00733
Known Genes
MethodMerging
AnalysisPhasedSV,MsPAC, Multiple Illumina callers, BioNano Genomics software
PlatformSee merged experiments
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3183514
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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