A curated catalogue of human genomic structural variation




Variant Details

Variant: essv5664448



Internal ID8641851
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:141411075..141411190hg38UCSC Ensembl
Outerchr7:141411038..141411240hg38UCSC Ensembl
Innerchr7:141110875..141110990hg19UCSC Ensembl
Outerchr7:141110838..141111040hg19UCSC Ensembl
Cytoband7q34
Allele length
AssemblyAllele length
hg38203
hg19203
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsesv2678484
Supporting Variants
SamplesHG00353
Known GenesTMEM178B
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv5664448
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer