A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2658525



Internal ID9924630
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:31903367..31911036hg38UCSC Ensembl
chr6:31871144..31878813hg19UCSC Ensembl
Cytoband6p21.33
Allele length
AssemblyAllele length
hg387670
hg197670
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv5660302, essv6596992, essv5818123, essv5822168, essv5560615, essv6177364, essv6392602, essv6268170, essv6465847, essv6045666, essv5694221
SamplesHG00542, NA19005, NA18619, NA20539, NA19725, NA18520, NA19456, NA18538, NA19338, NA19072, NA19080
Known GenesC2
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2658525
Frequency
Sample Size1151
Observed Gain0
Observed Loss11
Observed Complex0
Frequencyn/a


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