A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv8451n152



Internal ID22824154
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:29891112..29891178hg38UCSC Ensembl
chr7:29930728..29930794hg19UCSC Ensembl
Cytoband7p14.3
Allele length
AssemblyAllele length
hg3867
hg1967
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv3283993, nsv3288505
SamplesNA19240, HG00733
Known GenesWIPF3
MethodMerging
AnalysisPhasedSV,MsPAC, Multiple Illumina callers, BioNano Genomics software
PlatformSee merged experiments
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)dgv8451n152
Frequency
Sample Size9
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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