A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6024870



Internal ID9613665
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:23251597..23256951hg38UCSC Ensembl
Outerchr14:23251560..23257001hg38UCSC Ensembl
Innerchr14:23720806..23726160hg19UCSC Ensembl
Outerchr14:23720769..23726210hg19UCSC Ensembl
Cytoband14q11.2
Allele length
AssemblyAllele length
hg385442
hg195442
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsesv2658154
Supporting Variants
SamplesNA19315
Known GenesC14orf164
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv6024870
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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