A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6487584



Internal ID9464987
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:14539101..14542284hg38UCSC Ensembl
Outerchr19:14538944..14542437hg38UCSC Ensembl
Innerchr19:14649913..14653096hg19UCSC Ensembl
Outerchr19:14649756..14653249hg19UCSC Ensembl
Cytoband19p13.12
Allele length
AssemblyAllele length
hg383494
hg193494
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsesv2678628
Supporting Variants
SamplesNA18868
Known GenesTECR
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv6487584
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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