A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2661761



Internal ID9927866
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:45227375..45229133hg38UCSC Ensembl
chr15:45519573..45521331hg19UCSC Ensembl
Cytoband15q21.1
Allele length
AssemblyAllele length
hg381759
hg191759
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv6120108, essv5936082, essv6430386, essv6307080, essv5563777, essv6458179, essv5717593, essv6042285, essv5932948, essv5950368, essv5545129, essv6309685, essv5420394, essv6466008, essv5624706, essv5916146, essv5892958, essv5478153, essv5989037, essv6377929, essv6563925, essv5522067, essv5915103, essv5902746, essv5532353, essv5454380, essv6061820, essv5475718, essv6339042, essv5400977, essv6269233, essv6033011, essv5999397, essv5713284
SamplesNA18502, NA19914, NA19359, NA19092, NA19355, NA19819, NA19381, HG01167, NA18923, NA19130, NA18874, NA19917, NA19137, NA19159, NA19152, NA18871, NA19453, NA18912, NA19436, NA19440, NA19256, NA19147, NA19712, NA19434, NA19428, HG01108, NA18501, NA19223, NA20334, NA19093, NA20289, NA19711, NA19129, NA19316
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2661761
Frequency
Sample Size1151
Observed Gain0
Observed Loss34
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer