A curated catalogue of human genomic structural variation




Variant Details

Variant: essv5837450



Internal ID9656729
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:34818105..34818788hg38UCSC Ensembl
Outerchr19:34818068..34818838hg38UCSC Ensembl
Innerchr19:35309009..35309692hg19UCSC Ensembl
Outerchr19:35308972..35309742hg19UCSC Ensembl
Cytoband19q13.11
Allele length
AssemblyAllele length
hg38771
hg19771
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsesv2670616
Supporting Variants
SamplesNA19385
Known GenesLOC400685
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv5837450
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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