A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3644556



Internal ID6684623
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:47657354..47665879hg38UCSC Ensembl
Innerchr19:47657354..47665879hg38UCSC Ensembl
Outerchr19:47656854..47666379hg38UCSC Ensembl
chr19:48160611..48169136hg19UCSC Ensembl
Innerchr19:48160611..48169136hg19UCSC Ensembl
Outerchr19:48160111..48169636hg19UCSC Ensembl
Cytoband19q13.33
Allele length
AssemblyAllele length
hg388526
hg198526
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv16071056
SamplesHG02166
Known GenesGLTSCR1
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3644556
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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