A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6397203



Internal ID9374606
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:14641212..14642792hg38UCSC Ensembl
chr10:14683211..14684791hg19UCSC Ensembl
Cytoband10p13
Allele length
AssemblyAllele length
hg381581
hg191581
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsesv2658515
Supporting Variants
SamplesNA18964
Known GenesFAM107B
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv6397203
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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