A curated catalogue of human genomic structural variation




Variant Details

Variant: essv5955325



Internal ID9511573
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:41419863..41421752hg38UCSC Ensembl
chr15:41712061..41713950hg19UCSC Ensembl
Cytoband15q15.1
Allele length
AssemblyAllele length
hg381890
hg191890
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsesv2674168
Supporting Variants
SamplesNA18990
Known GenesRTF1
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv5955325
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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