A curated catalogue of human genomic structural variation




Variant Details

Variant: essv5942468



Internal ID8919871
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:29629592..29630062hg38UCSC Ensembl
chr10:29918521..29918991hg19UCSC Ensembl
Cytoband10p11.23
Allele length
AssemblyAllele length
hg38471
hg19471
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsesv2678748
Supporting Variants
SamplesHG00180
Known GenesSVIL
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv5942468
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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