A curated catalogue of human genomic structural variation




Variant Details

Variant: essv5632126



Internal ID8977033
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:109762986..109764612hg38UCSC Ensembl
chr7:109403043..109404669hg19UCSC Ensembl
Cytoband7q31.1
Allele length
AssemblyAllele length
hg381627
hg191627
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsesv2665727
Supporting Variants
SamplesHG00557
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv5632126
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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