A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6582699



Internal ID9560102
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:18381605..18382402hg38UCSC Ensembl
chr10:18670534..18671331hg19UCSC Ensembl
Cytoband10p12.32
Allele length
AssemblyAllele length
hg38798
hg19798
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsesv2675755
Supporting Variants
SamplesNA19445
Known GenesCACNB2
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv6582699
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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