A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6557388



Internal ID9893384
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:82992877..82998251hg38UCSC Ensembl
Outerchr4:82992720..82998404hg38UCSC Ensembl
Innerchr4:83914030..83919404hg19UCSC Ensembl
Outerchr4:83913873..83919557hg19UCSC Ensembl
Cytoband4q21.22
Allele length
AssemblyAllele length
hg385685
hg195685
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsesv2663118
Supporting Variants
SamplesNA20774
Known GenesLIN54
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv6557388
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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