A curated catalogue of human genomic structural variation




Variant Details

Variant: essv5953424



Internal ID8930827
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:46379456..46397406hg38UCSC Ensembl
Outerchr10:46379085..46397776hg38UCSC Ensembl
Innerchr10:47750716..47768672hg19UCSC Ensembl
Outerchr10:47750345..47769042hg19UCSC Ensembl
Cytoband10q11.22
Allele length
AssemblyAllele length
hg3818692
hg1918698
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsesv2664704
Supporting Variants
SamplesNA20322
Known GenesANXA8L1, ANXA8L2
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv5953424
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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