A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3631371



Internal ID7018180
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:18963951..19025554hg38UCSC Ensembl
chr13:19538091..19599694hg19UCSC Ensembl
Cytoband13q12.11
Allele length
AssemblyAllele length
hg3861604
hg1961604
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv14655482, essv14655475, essv14655477, essv14655476, essv14655480, essv14655478, essv14655483, essv14655479, essv14655481
SamplesHG02784, HG03016, HG03873, HG02780, NA21098, HG04176, NA21125, NA21088, HG03998
Known GenesLINC00442
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3631371
Frequency
Sample Size2504
Observed Gain0
Observed Loss9
Observed Complex0
Frequencyn/a


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