A curated catalogue of human genomic structural variation




Variant Details

Variant: essv5804598



Internal ID8782001
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:102328500..102381705hg38UCSC Ensembl
chr7:101968917..102022152hg19UCSC Ensembl
Cytoband7q22.1
Allele length
AssemblyAllele length
hg3853206
hg1953236
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsesv2673677
Supporting Variants
SamplesNA19374
Known GenesLOC100289561, LOC100630923, SPDYE6
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv5804598
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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