A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3636426



Internal ID6676533
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:49354085..49408851hg38UCSC Ensembl
chr15:49646282..49701048hg19UCSC Ensembl
Cytoband15q21.2
Allele length
AssemblyAllele length
hg3854767
hg1954767
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15245735, essv15245733, essv15245734
SamplesNA18621, HG02128, NA18971
Known GenesFAM227B
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3636426
Frequency
Sample Size2504
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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