A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3619527



Internal ID6659713
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:9799007..9828748hg38UCSC Ensembl
chr9:9799007..9828748hg19UCSC Ensembl
Cytoband9p23
Allele length
AssemblyAllele length
hg3829742
hg1929742
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1439e214
Supporting Variantsessv13396625, essv13396624
SamplesHG01524, NA11840
Known GenesPTPRD
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3619527
Frequency
Sample Size2504
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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