A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3643715



Internal ID6683786
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:12905367..12910805hg38UCSC Ensembl
Innerchr19:12905867..12910305hg38UCSC Ensembl
Outerchr19:12904367..12911805hg38UCSC Ensembl
chr19:13016181..13021619hg19UCSC Ensembl
Innerchr19:13016681..13021119hg19UCSC Ensembl
Outerchr19:13015181..13022619hg19UCSC Ensembl
Cytoband19p13.2
Allele length
AssemblyAllele length
hg385439
hg195439
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15995486
SamplesHG03123
Known GenesSYCE2
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3643715
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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