A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2658983



Internal ID9925088
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:144566323..144595667hg38UCSC Ensembl
Outerchr4:144566286..144595717hg38UCSC Ensembl
Innerchr4:145487475..145516819hg19UCSC Ensembl
Outerchr4:145487438..145516869hg19UCSC Ensembl
Cytoband4q31.21
Allele length
AssemblyAllele length
hg3829432
hg1929432
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv6186556
SamplesNA20276
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2658983
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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