A curated catalogue of human genomic structural variation




Variant Details

Variant: essv5955022



Internal ID8932425
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:4769607..4811637hg38UCSC Ensembl
Outerchr7:4769570..4811687hg38UCSC Ensembl
Innerchr7:4809238..4851268hg19UCSC Ensembl
Outerchr7:4809201..4851318hg19UCSC Ensembl
Cytoband7p22.1
Allele length
AssemblyAllele length
hg3842118
hg1942118
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsesv2664593
Supporting Variants
SamplesNA19711
Known GenesAP5Z1, FOXK1, MIR4656, RADIL
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv5955022
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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