A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3637939



Internal ID6678038
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:11772011..11773697hg38UCSC Ensembl
Innerchr16:11772056..11773653hg38UCSC Ensembl
Outerchr16:11771967..11773742hg38UCSC Ensembl
chr16:11865867..11867553hg19UCSC Ensembl
Innerchr16:11865912..11867509hg19UCSC Ensembl
Outerchr16:11865823..11867598hg19UCSC Ensembl
Cytoband16p13.13
Allele length
AssemblyAllele length
hg381687
hg191687
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15377073, essv15377079, essv15377032, essv15377027, essv15377037, essv15377067, essv15377050, essv15377075, essv15377076, essv15377042, essv15377043, essv15377025, essv15377064, essv15377055, essv15377068, essv15377048, essv15377071, essv15377074, essv15377056, essv15377054, essv15377026, essv15377059, essv15377030, essv15377044, essv15377080, essv15377035, essv15377069, essv15377072, essv15377081, essv15377038, essv15377065, essv15377034, essv15377040, essv15377078, essv15377041, essv15377060, essv15377045, essv15377028, essv15377049, essv15377070, essv15377066, essv15377053, essv15377036, essv15377082, essv15377058, essv15377046, essv15377039, essv15377063, essv15377031, essv15377083, essv15377077, essv15377057, essv15377033, essv15377061, essv15377052, essv15377051, essv15377047, essv15377062, essv15377029
SamplesHG02496, NA19913, HG02107, HG03160, NA20351, NA19904, HG02970, HG03382, HG03304, HG03295, NA19223, NA20299, HG02979, NA19430, NA18877, HG03046, HG03265, HG01167, HG03294, HG03103, NA19257, NA19108, HG01990, NA19236, HG03199, HG02976, NA18505, HG03457, HG03159, HG02420, NA18912, NA19982, HG03451, NA19107, HG03439, NA19096, NA19908, HG03520, HG03100, NA19256, HG01986, NA19042, NA19247, NA19372, HG02054, HG03397, NA19102, NA19119, HG02501, HG03499, NA20332, NA19116, HG02144, HG02481, HG02256, HG02476, NA19315, HG03117, HG02095
Known GenesZC3H7A
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3637939
Frequency
Sample Size2504
Observed Gain0
Observed Loss59
Observed Complex0
Frequencyn/a


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