A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6441040



Internal ID9063796
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:38740243..38744491hg38UCSC Ensembl
Outerchr14:38740086..38744644hg38UCSC Ensembl
Innerchr14:39209447..39213695hg19UCSC Ensembl
Outerchr14:39209290..39213848hg19UCSC Ensembl
Cytoband14q21.1
Allele length
AssemblyAllele length
hg384559
hg194559
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsesv2663045
Supporting Variants
SamplesHG00708
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv6441040
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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