A curated catalogue of human genomic structural variation




Variant Details

Variant: essv5986902



Internal ID8964305
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
SamplesNA07347
Known GenesTMEM178B
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv5986902
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