A curated catalogue of human genomic structural variation




Variant Details

Variant: essv15245733



Internal ID5247549
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 StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3636426
Supporting Variants
SamplesHG02128
Known GenesFAM227B
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv15245733
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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