A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2673357



Internal ID9939462
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:19963526..20570323hg38UCSC Ensembl
Outerchr19:19963492..20570358hg38UCSC Ensembl
Innerchr19:20074335..20753129hg19UCSC Ensembl
Outerchr19:20074301..20753164hg19UCSC Ensembl
Cytoband19p12
Allele length
AssemblyAllele length
hg38606867
hg19678864
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv630e199
Supporting Variantsessv5693101
SamplesHG00148
Known GenesMIR1270-1, MIR1270-2, ZNF486, ZNF682, ZNF737, ZNF826P, ZNF90
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2673357
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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