A curated catalogue of human genomic structural variation




Variant Details

Variant: essv5488554



Internal ID8465957
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:46373257..46397356hg38UCSC Ensembl
Outerchr10:46372885..46397726hg38UCSC Ensembl
Innerchr10:47744516..47768622hg19UCSC Ensembl
Outerchr10:47744145..47768992hg19UCSC Ensembl
Cytoband10q11.22
Allele length
AssemblyAllele length
hg3824842
hg1924848
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsesv2661207
Supporting Variants
SamplesNA19777
Known GenesANXA8L1, ANXA8L2, FAM25B
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv5488554
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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