A curated catalogue of human genomic structural variation




Variant Details

Variant: essv5716709



Internal ID9748534
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:13166142..13166551hg38UCSC Ensembl
Outerchr19:13166105..13166601hg38UCSC Ensembl
Innerchr19:13276956..13277365hg19UCSC Ensembl
Outerchr19:13276919..13277415hg19UCSC Ensembl
Cytoband19p13.2
Allele length
AssemblyAllele length
hg38497
hg19497
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2671928
Supporting Variants
SamplesNA19700
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv5716709
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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