A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2665674



Internal ID9931779
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:34412110..34412270hg38UCSC Ensembl
Outerchr14:34411950..34412437hg38UCSC Ensembl
Innerchr14:34881316..34881476hg19UCSC Ensembl
Outerchr14:34881156..34881643hg19UCSC Ensembl
Cytoband14q13.1
Allele length
AssemblyAllele length
hg38488
hg19488
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv6411435, essv6333857, essv6017792, essv5508596, essv6263978, essv6550657, essv6170090, essv5422249, essv5652414, essv6414742, essv5617418, essv6359392, essv6327117, essv6470927, essv6240816, essv5436942, essv5848594, essv5854611, essv5595775, essv5436109, essv5625083, essv5598613, essv6376061, essv5464623, essv6195443, essv5730787, essv5727127, essv6107351, essv5718320, essv6139583, essv5908950, essv5796663, essv6437072, essv6369445, essv6096254, essv6095345, essv6061090, essv6283326, essv6544889, essv5916105, essv6106769, essv6412552, essv6018976, essv5404422, essv5909402, essv6254646, essv6434613, essv6478972, essv6186468
SamplesNA19394, NA19703, HG01462, HG00524, NA19399, NA18565, HG01374, NA18999, NA19819, NA19393, NA19377, NA19920, NA19381, NA19379, NA18619, HG01083, HG01365, NA19404, HG01170, NA19371, HG00534, HG01440, HG00182, NA18985, HG01136, NA19082, HG01171, HG00328, NA19391, HG00344, HG00708, HG01390, HG01073, HG00613, NA18523, HG00463, NA18542, NA19834, NA19712, HG00375, NA19380, HG01174, NA19439, NA19311, HG01137, NA19818, NA19312, NA19463, NA18620
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2665674
Frequency
Sample Size1151
Observed Gain0
Observed Loss49
Observed Complex0
Frequencyn/a


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