A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2662926



Internal ID9582345
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:214371..339491hg38UCSC Ensembl
Outerchr4:214304..339559hg38UCSC Ensembl
Innerchr4:208160..333280hg19UCSC Ensembl
Outerchr4:208093..333348hg19UCSC Ensembl
Cytoband4p16.3
Allele length
AssemblyAllele length
hg38125256
hg19125256
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv914e199
Supporting Variantsessv6019379, essv6496643, essv5999794
SamplesNA19379, HG00266, HG01048
Known GenesZNF141, ZNF732, ZNF876P
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2662926
Frequency
Sample Size1151
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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