A curated catalogue of human genomic structural variation




Variant Details

Variant: essv5396022



Internal ID8373425
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:135149105..135156337hg38UCSC Ensembl
Outerchr7:135149068..135156387hg38UCSC Ensembl
Innerchr7:134833857..134841089hg19UCSC Ensembl
Outerchr7:134833820..134841139hg19UCSC Ensembl
Cytoband7q33
Allele length
AssemblyAllele length
hg387320
hg197320
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsesv2665250
Supporting Variants
SamplesNA18633
Known GenesTMEM140
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv5396022
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