A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2673570



Internal ID9939675
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:103117193..103117481hg38UCSC Ensembl
chr14:103583530..103583818hg19UCSC Ensembl
Cytoband14q32.32
Allele length
AssemblyAllele length
hg38289
hg19289
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv5659001, essv5693141, essv6389878, essv6491614, essv5443764, essv5649548
SamplesHG01069, HG00282, HG00320, HG00250, HG00125, HG00329
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2673570
Frequency
Sample Size1151
Observed Gain0
Observed Loss6
Observed Complex0
Frequencyn/a


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