A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3644534



Internal ID7031289
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:46666730..46671540hg38UCSC Ensembl
Innerchr19:46666736..46671535hg38UCSC Ensembl
Outerchr19:46666725..46671546hg38UCSC Ensembl
chr19:47169987..47174797hg19UCSC Ensembl
Innerchr19:47169993..47174792hg19UCSC Ensembl
Outerchr19:47169982..47174803hg19UCSC Ensembl
Cytoband19q13.32
Allele length
AssemblyAllele length
hg384811
hg194811
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv16069688, essv16069687
SamplesHG00367, HG01248
Known GenesDACT3-AS1
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3644534
Frequency
Sample Size2504
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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