A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2671551



Internal ID9937656
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:9380062..9380304hg38UCSC Ensembl
Outerchr1:9379905..9380457hg38UCSC Ensembl
Innerchr1:9440121..9440363hg19UCSC Ensembl
Outerchr1:9439964..9440516hg19UCSC Ensembl
Cytoband1p36.22
Allele length
AssemblyAllele length
hg38553
hg19553
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv5675200, essv6360424, essv6310252, essv5936819, essv6192437, essv5886599, essv5835426, essv6387779, essv6217017, essv5803169, essv6306689, essv5617422, essv6064542, essv6081254, essv5565537, essv5920208, essv6215876, essv6584703, essv5769749, essv6383000
SamplesNA19397, NA19399, NA19350, NA18504, NA19684, NA19396, NA19379, NA19448, NA19172, HG00731, NA19391, NA18516, NA18871, NA19099, NA19625, HG01551, HG00638, HG01342, NA19472, NA20334
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2671551
Frequency
Sample Size1151
Observed Gain0
Observed Loss20
Observed Complex0
Frequencyn/a


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