A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv1240e199



Internal ID20124542
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:134538191..134577348hg38UCSC Ensembl
chr7:134222943..134262100hg19UCSC Ensembl
Cytoband7q33
Allele length
AssemblyAllele length
hg3839158
hg1939158
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsesv2666945, esv2672772
SamplesHG00359, NA18528
Known GenesAKR1B10, AKR1B15
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)dgv1240e199
Frequency
Sample Size1151
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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