A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6491614



Internal ID9087720
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 StatusS
Merged Variantsesv2673570
Supporting Variants
SamplesHG01069
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv6491614
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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