A curated catalogue of human genomic structural variation




Variant Details

Variant: essv5688871



Internal ID8666274
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:111799312..111816910hg38UCSC Ensembl
Outerchr1:111799275..111816960hg38UCSC Ensembl
Innerchr1:112341934..112359532hg19UCSC Ensembl
Outerchr1:112341897..112359582hg19UCSC Ensembl
Cytoband1p13.2
Allele length
AssemblyAllele length
hg3817686
hg1917686
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsesv2675358
Supporting Variants
SamplesHG00626
Known GenesKCND3
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv5688871
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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