A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3178378



Internal ID22334952
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:141703338..141709325hg38UCSC Ensembl
chr7:141403138..141409125hg19UCSC Ensembl
Cytoband7q34
Allele length
AssemblyAllele length
hg385988
hg195988
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14402634
SamplesNA19240
Known GenesWEE2, WEE2-AS1
MethodMerging
AnalysisPhasedSV,MsPAC, Multiple Illumina callers, BioNano Genomics software
PlatformSee merged experiments
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3178378
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