A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6237629



Internal ID9365941
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:70580454..70582572hg38UCSC Ensembl
chr14:71047171..71049289hg19UCSC Ensembl
Cytoband14q24.2
Allele length
AssemblyAllele length
hg382119
hg192119
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsesv2675400
Supporting Variants
SamplesNA18560
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv6237629
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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