A curated catalogue of human genomic structural variation




Variant Details

Variant: essv5739337



Internal ID8716740
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:11928601..11935157hg38UCSC Ensembl
Outerchr19:11928230..11935777hg38UCSC Ensembl
Innerchr19:12039416..12045972hg19UCSC Ensembl
Outerchr19:12039045..12046592hg19UCSC Ensembl
Cytoband19p13.2
Allele length
AssemblyAllele length
hg387548
hg197548
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsesv2678865
Supporting Variants
SamplesNA18916
Known GenesZNF700
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv5739337
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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