A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv1193e199



Internal ID22758966
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:37653769..37665558hg38UCSC Ensembl
chr7:37693372..37705161hg19UCSC Ensembl
Cytoband7p14.1
Allele length
AssemblyAllele length
hg3811790
hg1911790
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsesv2660500, esv2663009
SamplesNA19359
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)dgv1193e199
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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