A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3635989



Internal ID7022786
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:28108015..28121432hg38UCSC Ensembl
chr15:28353161..28366578hg19UCSC Ensembl
Cytoband15q13.1
Allele length
AssemblyAllele length
hg3813418
hg1913418
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15198888, essv15198890, essv15198887, essv15198893, essv15198889, essv15198894, essv15198891, essv15198892
SamplesHG00634, HG00610, HG00629, HG00266, HG00404, NA12272, HG00112, HG00628
Known GenesHERC2
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3635989
Frequency
Sample Size2504
Observed Gain0
Observed Loss8
Observed Complex0
Frequencyn/a


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