A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2672275



Internal ID9938380
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:62532703..62816176hg38UCSC Ensembl
chr6:63242608..63526081hg19UCSC Ensembl
Cytoband6q11.1
Allele length
AssemblyAllele length
hg38283474
hg19283474
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv6549091, essv6090562, essv6434634
SamplesHG00608, NA19469, HG00377
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2672275
Frequency
Sample Size1151
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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