A curated catalogue of human genomic structural variation




Variant Details

Variant: essv5851128



Internal ID8828531
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:114313446..114313758hg38UCSC Ensembl
chr7:113953501..113953813hg19UCSC Ensembl
Cytoband7q31.1
Allele length
AssemblyAllele length
hg38313
hg19313
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2677382
Supporting Variants
SamplesNA18633
Known GenesFOXP2
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv5851128
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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