A curated catalogue of human genomic structural variation




Variant Details

Variant: essv5640031



Internal ID8830208
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:131110795..131114516hg38UCSC Ensembl
chr10:132909058..132912779hg19UCSC Ensembl
Cytoband10q26.3
Allele length
AssemblyAllele length
hg383722
hg193722
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsesv2669390
Supporting Variants
SamplesHG00270
Known GenesTCERG1L
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv5640031
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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