A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6119261



Internal ID9217786
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 Variantsesv2658017
Supporting Variants
SamplesNA07357
Known GenesTCERG1L
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv6119261
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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