A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv8602n152



Internal ID22824305
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:75048266..75058095hg38UCSC Ensembl
chr7:74462375..74472202hg19UCSC Ensembl
Cytoband7q11.23
Allele length
AssemblyAllele length
hg389830
hg199828
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv3210085, nsv3201150
SamplesNA19240
Known GenesWBSCR16
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)dgv8602n152
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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