A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3643452



Internal ID7030214
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:3037480..3040988hg38UCSC Ensembl
Innerchr19:3037530..3040938hg38UCSC Ensembl
Outerchr19:3037429..3041039hg38UCSC Ensembl
chr19:3037478..3040986hg19UCSC Ensembl
Innerchr19:3037528..3040936hg19UCSC Ensembl
Outerchr19:3037427..3041037hg19UCSC Ensembl
Cytoband19p13.3
Allele length
AssemblyAllele length
hg383509
hg193509
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15974447
SamplesHG01438
Known GenesTLE2
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3643452
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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