A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6270863



Internal ID9248266
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:6968239..6968760hg38UCSC Ensembl
Outerchr19:6968202..6968810hg38UCSC Ensembl
Innerchr19:6968250..6968771hg19UCSC Ensembl
Outerchr19:6968213..6968821hg19UCSC Ensembl
Cytoband19p13.2
Allele length
AssemblyAllele length
hg38609
hg19609
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsesv2668680
Supporting Variants
SamplesNA19452
Known GenesEMR4P
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv6270863
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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