A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv1212e199



Internal ID22758985
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:64022454..64329639hg38UCSC Ensembl
chr7:63482832..63790017hg19UCSC Ensembl
Cytoband7q11.21
Allele length
AssemblyAllele length
hg38307186
hg19307186
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsesv2659946, esv2664319, esv2675550
SamplesHG01462, NA20507, NA18532, NA19012, HG01061
Known GenesLINC01005, ZNF679, ZNF727, ZNF735, ZNF736
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)dgv1212e199
Frequency
Sample Size1151
Observed Gain0
Observed Loss5
Observed Complex0
Frequencyn/a


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