A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2668750



Internal ID9934855
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:24529667..24535142hg38UCSC Ensembl
Outerchr16:24529628..24535199hg38UCSC Ensembl
Innerchr16:24540988..24546463hg19UCSC Ensembl
Outerchr16:24540949..24546520hg19UCSC Ensembl
Cytoband16p12.1
Allele length
AssemblyAllele length
hg385572
hg195572
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv488e199
Supporting Variantsessv6260424, essv6524112, essv6322196, essv5483310, essv5886083, essv5991946, essv5432771, essv5885059, essv6052984, essv5433751, essv6076476, essv5861821, essv6555161, essv5516841, essv5400465, essv5879190, essv5488998, essv5639967, essv5822384, essv6065492, essv5458078, essv5580133, essv6260360, essv6002814, essv6454056, essv6385314, essv6364664, essv6222088, essv6045098, essv5596584, essv5677100, essv6531911, essv5789074, essv6011411, essv6257204
SamplesNA19397, NA18924, NA19204, NA18508, NA18486, NA20294, NA19355, NA19377, NA19098, NA19396, NA19201, NA20586, NA19404, NA19137, NA19207, NA19172, NA19901, NA18520, NA20342, NA19445, NA18934, NA19982, NA18907, NA19114, NA18853, NA19099, NA18523, NA20296, NA19434, NA19360, NA19328, NA19223, NA19102, NA19316, NA18522
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2668750
Frequency
Sample Size1151
Observed Gain0
Observed Loss35
Observed Complex0
Frequencyn/a


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