A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2669622



Internal ID9935727
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:154991201..154993038hg38UCSC Ensembl
chr6:155312335..155314172hg19UCSC Ensembl
Cytoband6q25.2
Allele length
AssemblyAllele length
hg381838
hg191838
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv6527978, essv6197906, essv6521592, essv5674291, essv5498981, essv6189517, essv6327345, essv6136194, essv5492136, essv5839480, essv6234524, essv6122982, essv6203167, essv6264813, essv6421822, essv6473242, essv5552167, essv6032907, essv5421551, essv6118455, essv5462002, essv5962012, essv5401484, essv6073773, essv5697673, essv6497977, essv5748973, essv5899219, essv6269430
SamplesNA12273, NA20816, NA20512, NA12750, NA19381, HG00122, NA20589, NA20795, HG01072, HG00160, HG00253, NA20515, NA10847, NA20535, HG01171, HG00245, NA19788, NA19776, NA20765, HG00254, HG01190, NA19380, HG01174, HG01108, NA07037, HG00259, NA20528, HG00372, NA19429
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2669622
Frequency
Sample Size1151
Observed Gain0
Observed Loss29
Observed Complex0
Frequencyn/a


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