A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3638153



Internal ID7024939
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:20698114..20701665hg38UCSC Ensembl
Innerchr16:20698149..20701631hg38UCSC Ensembl
Outerchr16:20698080..20701700hg38UCSC Ensembl
chr16:20709436..20712987hg19UCSC Ensembl
Innerchr16:20709471..20712953hg19UCSC Ensembl
Outerchr16:20709402..20713022hg19UCSC Ensembl
Cytoband16p12.3
Allele length
AssemblyAllele length
hg383552
hg193552
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15404978, essv15405000, essv15405005, essv15404989, essv15404999, essv15404985, essv15405008, essv15405011, essv15405020, essv15405021, essv15405013, essv15404998, essv15405009, essv15404987, essv15405006, essv15404995, essv15404982, essv15405016, essv15405022, essv15404984, essv15404979, essv15404991, essv15405002, essv15404993, essv15405003, essv15405012, essv15405001, essv15405025, essv15405017, essv15404983, essv15404994, essv15404988, essv15405004, essv15404996, essv15405024, essv15404980, essv15405015, essv15405014, essv15404992, essv15405019, essv15404997, essv15405010, essv15405007, essv15405026, essv15404977, essv15405018, essv15404986, essv15404981, essv15404990, essv15405023
SamplesHG02784, HG03738, HG02691, HG02688, HG03705, HG02690, NA20890, HG03808, HG03874, NA21108, HG03911, NA20910, HG03803, HG03897, HG04106, HG03777, HG03784, HG03780, HG03785, HG03714, HG04225, HG04062, HG03775, HG03919, HG03660, HG03643, HG04189, HG04063, HG03969, HG03774, NA20872, HG04025, HG03598, HG04134, NA20902, NA21095, HG03846, HG03703, HG03729, HG04023, NA21088, HG03977, NA20849, HG03733, HG01846, HG03998, HG03925, HG04061, HG03931, HG03686
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3638153
Frequency
Sample Size2504
Observed Gain0
Observed Loss50
Observed Complex0
Frequencyn/a


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