A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2664107



Internal ID9583526
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:1368119..1368256hg38UCSC Ensembl
chr10:1410314..1410451hg19UCSC Ensembl
Cytoband10p15.3
Allele length
AssemblyAllele length
hg38138
hg19138
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv6072016, essv5881063, essv5675398, essv6253675, essv6185466, essv5928589, essv6360060
SamplesNA07347, HG01052, HG00253, HG00154, HG01107, HG01073, NA11992
Known GenesADARB2
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2664107
Frequency
Sample Size1151
Observed Gain0
Observed Loss7
Observed Complex0
Frequencyn/a


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