A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6362026



Internal ID9142901
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:9449105..9454535hg38UCSC Ensembl
chr10:9491068..9496498hg19UCSC Ensembl
Cytoband10p14
Allele length
AssemblyAllele length
hg385431
hg195431
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsesv2676973
Supporting Variants
SamplesHG01190
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv6362026
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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