A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6062814



Internal ID9040217
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:42112737..42113887hg38UCSC Ensembl
chr12:42506539..42507689hg19UCSC Ensembl
Cytoband12q12
Allele length
AssemblyAllele length
hg381151
hg191151
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2665869
Supporting Variants
SamplesNA19235
Known GenesGXYLT1
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv6062814
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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