A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3644252



Internal ID7031008
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:36257038..36268344hg38UCSC Ensembl
Innerchr19:36257538..36267844hg38UCSC Ensembl
Outerchr19:36256038..36269344hg38UCSC Ensembl
chr19:36747940..36759246hg19UCSC Ensembl
Innerchr19:36748440..36758746hg19UCSC Ensembl
Outerchr19:36746940..36760246hg19UCSC Ensembl
Cytoband19q13.12
Allele length
AssemblyAllele length
hg3811307
hg1911307
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv16048768
SamplesHG00530
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3644252
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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