A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2676076



Internal ID9942181
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:105784438..105785894hg38UCSC Ensembl
Outerchr8:105784067..105786264hg38UCSC Ensembl
Innerchr8:106796666..106798122hg19UCSC Ensembl
Outerchr8:106796295..106798492hg19UCSC Ensembl
Cytoband8q23.1
Allele length
AssemblyAllele length
hg382198
hg192198
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv6453698, essv5551835, essv5472019, essv5666375, essv5598435, essv5444272, essv6383784, essv5704323, essv5920944, essv6538227, essv6459998, essv5934597, essv6500257, essv6116878, essv5422825, essv6069140, essv5730368, essv6212786, essv6591462, essv6265209, essv6509131, essv6559819, essv5949188, essv6598216, essv5709429, essv5560355, essv6254819, essv5955722, essv6058516, essv6416185, essv6478774, essv5426087, essv6477067, essv6408811
SamplesNA19394, NA19332, NA19355, NA19381, NA19379, NA19319, NA19382, NA19448, NA19372, NA19371, NA19317, NA19456, NA19437, NA19347, NA19461, NA19449, NA19338, NA19452, NA19469, NA19390, NA19473, NA19435, NA19331, NA19334, NA19470, NA19467, NA19328, NA19438, NA19472, NA19468, NA19474, NA19430, NA19316, NA19431
Known GenesZFPM2
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2676076
Frequency
Sample Size1151
Observed Gain0
Observed Loss34
Observed Complex0
Frequencyn/a


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