A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2671358



Internal ID9590777
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:14052861..14055035hg38UCSC Ensembl
Outerchr10:14052704..14055188hg38UCSC Ensembl
Innerchr10:14094860..14097034hg19UCSC Ensembl
Outerchr10:14094703..14097187hg19UCSC Ensembl
Cytoband10p13
Allele length
AssemblyAllele length
hg382485
hg192485
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv121e199
Supporting Variantsessv5695867, essv6380068
SamplesNA19471, NA19439
Known GenesFRMD4A
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2671358
Frequency
Sample Size1151
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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