A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv8705n152



Internal ID22824408
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:107976854..107976931hg38UCSC Ensembl
chr7:107617299..107617376hg19UCSC Ensembl
Cytoband7q31.1
Allele length
AssemblyAllele length
hg3878
hg1978
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv3286890, nsv3199703, nsv3196900
SamplesHG00731, HG00732, NA19240, HG00733
Known GenesLAMB1
MethodMerging
Sequencing
AnalysisMultiple analysis algorthms
PhasedSV,MsPAC, Multiple Illumina callers, BioNano Genomics software
PlatformIllumina HiSeq
See merged experiments
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)dgv8705n152
Frequency
Sample Size9
Observed Gain0
Observed Loss4
Observed Complex0
Frequencyn/a


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