A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3632520



Internal ID7019330
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:66668408..66753143hg38UCSC Ensembl
chr13:67242540..67327275hg19UCSC Ensembl
Cytoband13q21.32
Allele length
AssemblyAllele length
hg3884736
hg1984736
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv341e214
Supporting Variantsessv14778098, essv14778097
SamplesNA18592, NA20849
Known GenesPCDH9
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3632520
Frequency
Sample Size2504
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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