A curated catalogue of human genomic structural variation




Variant Details

Variant: essv5525821



Internal ID9802121
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:10007221..10008579hg38UCSC Ensembl
Outerchr1:10007064..10008732hg38UCSC Ensembl
Innerchr1:10067279..10068637hg19UCSC Ensembl
Outerchr1:10067122..10068790hg19UCSC Ensembl
Cytoband1p36.22
Allele length
AssemblyAllele length
hg381669
hg191669
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsesv2671412
Supporting Variants
SamplesNA19835
Known GenesRBP7
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv5525821
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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