A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv8665n152



Internal ID22824368
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:99190284..99190717hg38UCSC Ensembl
chr7:98787907..98788340hg19UCSC Ensembl
Cytoband7q22.1
Allele length
AssemblyAllele length
hg38434
hg19434
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv3195710, nsv3206830
SamplesNA19238, NA19239, HG00732, HG00733, HG00514
Known GenesKPNA7
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)dgv8665n152
Frequency
Sample Size9
Observed Gain0
Observed Loss5
Observed Complex0
Frequencyn/a


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