A curated catalogue of human genomic structural variation




Variant Details

Variant: essv5874580



Internal ID8851983
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:173545502..173555526hg38UCSC Ensembl
Outerchr4:173545465..173555576hg38UCSC Ensembl
Innerchr4:174466653..174476677hg19UCSC Ensembl
Outerchr4:174466616..174476727hg19UCSC Ensembl
Cytoband4q34.1
Allele length
AssemblyAllele length
hg3810112
hg1910112
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsesv2670690
Supporting Variants
SamplesNA19395
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv5874580
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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