A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3644151



Internal ID7030907
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:31540012..31541427hg38UCSC Ensembl
Innerchr19:31540062..31541377hg38UCSC Ensembl
Outerchr19:31539906..31541533hg38UCSC Ensembl
chr19:32030918..32032333hg19UCSC Ensembl
Innerchr19:32030968..32032283hg19UCSC Ensembl
Outerchr19:32030812..32032439hg19UCSC Ensembl
Cytoband19q12
Allele length
AssemblyAllele length
hg381416
hg191416
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv16039946
SamplesHG04227
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3644151
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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