A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3644124



Internal ID7030880
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:29396790..29400455hg38UCSC Ensembl
Innerchr19:29396798..29400447hg38UCSC Ensembl
Outerchr19:29396782..29400463hg38UCSC Ensembl
chr19:29887697..29891362hg19UCSC Ensembl
Innerchr19:29887705..29891354hg19UCSC Ensembl
Outerchr19:29887689..29891370hg19UCSC Ensembl
Cytoband19q12
Allele length
AssemblyAllele length
hg383666
hg193666
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv16032722
SamplesNA21115
Known GenesLOC284395
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3644124
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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