A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6164807



Internal ID8948322
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:16941093..16949699hg38UCSC Ensembl
Outerchr4:16940722..16950069hg38UCSC Ensembl
Innerchr4:16942716..16951322hg19UCSC Ensembl
Outerchr4:16942345..16951692hg19UCSC Ensembl
Cytoband4p15.32
Allele length
AssemblyAllele length
hg389348
hg199348
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsesv2669072
Supporting Variants
SamplesHG00479
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv6164807
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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