A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv7961n152



Internal ID22823664
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:71316334..71316502hg38UCSC Ensembl
chr6:72026037..72026205hg19UCSC Ensembl
Cytoband6q13
Allele length
AssemblyAllele length
hg38169
hg19169
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv3191515, nsv3202253
SamplesHG00733
Known Genes
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)dgv7961n152
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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