A curated catalogue of human genomic structural variation




Variant Details

Variant: essv5793826



Internal ID9406218
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:35136660..35146366hg38UCSC Ensembl
Outerchr14:35136239..35146786hg38UCSC Ensembl
Innerchr14:35605866..35615572hg19UCSC Ensembl
Outerchr14:35605445..35615992hg19UCSC Ensembl
Cytoband14q13.2
Allele length
AssemblyAllele length
hg3810548
hg1910548
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsesv2664067
Supporting Variants
SamplesNA18610
Known GenesKIAA0391
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv5793826
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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