A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2666337



Internal ID9932442
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:39656846..39656952hg38UCSC Ensembl
Outerchr4:39656475..39657322hg38UCSC Ensembl
Innerchr4:39658466..39658572hg19UCSC Ensembl
Outerchr4:39658095..39658942hg19UCSC Ensembl
Cytoband4p14
Allele length
AssemblyAllele length
hg38848
hg19848
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv6527536, essv6123285, essv6434217, essv6404371, essv5965128, essv5907911, essv5824574, essv6260144, essv6318352, essv6365991, essv6215955, essv6030085, essv6595597, essv5431019, essv5634807, essv5630065, essv5965949, essv6087873, essv5727381, essv6141167, essv5582548, essv6122474, essv5858482, essv6057521, essv5500415, essv6061959, essv5502576
SamplesNA19648, NA19664, NA19678, NA19723, NA19771, NA19782, NA19651, NA19719, NA19725, NA19789, NA19657, NA19717, NA19663, NA19776, NA19654, NA19774, NA19655, NA19750, NA19756, NA19685, NA19749, NA19773, NA19770, NA19726, NA19780, NA19661, NA19676
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2666337
Frequency
Sample Size1151
Observed Gain0
Observed Loss27
Observed Complex0
Frequencyn/a


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