A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3643548



Internal ID6683619
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:6255988..6257576hg38UCSC Ensembl
Innerchr19:6256042..6257522hg38UCSC Ensembl
Outerchr19:6255934..6257630hg38UCSC Ensembl
chr19:6255999..6257587hg19UCSC Ensembl
Innerchr19:6256053..6257533hg19UCSC Ensembl
Outerchr19:6255945..6257641hg19UCSC Ensembl
Cytoband19p13.3
Allele length
AssemblyAllele length
hg381589
hg191589
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15985830
SamplesHG01851
Known GenesMLLT1
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3643548
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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