A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6577820



Internal ID9526723
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:105466276..105467980hg38UCSC Ensembl
Outerchr4:105466119..105468133hg38UCSC Ensembl
Innerchr4:106387433..106389137hg19UCSC Ensembl
Outerchr4:106387276..106389290hg19UCSC Ensembl
Cytoband4q24
Allele length
AssemblyAllele length
hg382015
hg192015
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsesv2667301
Supporting Variants
SamplesNA19056
Known GenesPPA2
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv6577820
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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