A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3643416



Internal ID6683491
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:1989080..1999559hg38UCSC Ensembl
chr19:1989079..1999558hg19UCSC Ensembl
Cytoband19p13.3
Allele length
AssemblyAllele length
hg3810480
hg1910480
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15968883, essv15968882
SamplesHG02546, HG02455
Known GenesBTBD2
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3643416
Frequency
Sample Size2504
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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