A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2674048



Internal ID9593467
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:16609570..16610047hg38UCSC Ensembl
Outerchr19:16609533..16610097hg38UCSC Ensembl
Innerchr19:16720381..16720858hg19UCSC Ensembl
Outerchr19:16720344..16720908hg19UCSC Ensembl
Cytoband19p13.11
Allele length
AssemblyAllele length
hg38565
hg19565
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv6588806
SamplesNA18523
Known GenesMED26
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2674048
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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