A curated catalogue of human genomic structural variation




Variant Details

Variant: essv5713474



Internal ID9658211
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:74365191..74366607hg38UCSC Ensembl
Outerchr14:74365034..74366760hg38UCSC Ensembl
Innerchr14:74831894..74833310hg19UCSC Ensembl
Outerchr14:74831737..74833463hg19UCSC Ensembl
Cytoband14q24.3
Allele length
AssemblyAllele length
hg381727
hg191727
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2675639
Supporting Variants
SamplesNA19390
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv5713474
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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