A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3189104



Internal ID22340604
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:134920257..134920346hg38UCSC Ensembl
chr7:134605008..134605097hg19UCSC Ensembl
Cytoband7q33
Allele length
AssemblyAllele length
hg3890
hg1990
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14435893
SamplesHG00514
Known GenesCALD1
MethodMerging
AnalysisPhasedSV,MsPAC, Multiple Illumina callers, BioNano Genomics software
PlatformSee merged experiments
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3189104
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