A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6145905



Internal ID9123308
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:21525082..21526988hg38UCSC Ensembl
Outerchr14:21524711..21527358hg38UCSC Ensembl
Innerchr14:21993216..21995122hg19UCSC Ensembl
Outerchr14:21992845..21995492hg19UCSC Ensembl
Cytoband14q11.2
Allele length
AssemblyAllele length
hg382648
hg192648
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsesv2660046
Supporting Variants
SamplesNA19762
Known GenesSALL2
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv6145905
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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