A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2658783



Internal ID9924888
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:180545409..180551950hg38UCSC Ensembl
Outerchr4:180545372..180552000hg38UCSC Ensembl
Innerchr4:181466562..181473103hg19UCSC Ensembl
Outerchr4:181466525..181473153hg19UCSC Ensembl
Cytoband4q34.3
Allele length
AssemblyAllele length
hg386629
hg196629
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv5795124
SamplesNA18532
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2658783
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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