A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3639845



Internal ID7026623
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:6746603..6747667hg38UCSC Ensembl
Innerchr17:6746639..6747632hg38UCSC Ensembl
Outerchr17:6746568..6747703hg38UCSC Ensembl
chr17:6649922..6650986hg19UCSC Ensembl
Innerchr17:6649958..6650951hg19UCSC Ensembl
Outerchr17:6649887..6651022hg19UCSC Ensembl
Cytoband17p13.1
Allele length
AssemblyAllele length
hg381065
hg191065
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15602746, essv15602727, essv15602748, essv15602747, essv15602725, essv15602741, essv15602722, essv15602713, essv15602730, essv15602740, essv15602709, essv15602723, essv15602736, essv15602735, essv15602739, essv15602715, essv15602719, essv15602721, essv15602749, essv15602729, essv15602714, essv15602711, essv15602712, essv15602717, essv15602743, essv15602742, essv15602724, essv15602728, essv15602737, essv15602718, essv15602734, essv15602731, essv15602708, essv15602707, essv15602720, essv15602732, essv15602710, essv15602745, essv15602733, essv15602744, essv15602726, essv15602716, essv15602738
SamplesHG02614, HG02574, NA19466, HG02702, NA18877, HG02804, HG02536, HG02895, NA19171, HG02756, HG02549, NA20278, HG03268, HG03212, NA19471, HG03225, HG03058, HG02715, NA19437, HG03511, HG03088, HG02511, HG01879, HG01880, HG03027, HG02881, HG01890, HG02896, HG01990, HG02484, HG03567, NA19834, HG02983, HG02721, HG02982, HG03112, HG03025, HG03063, HG02013, NA18876, HG03401, HG03439, HG03265
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3639845
Frequency
Sample Size2504
Observed Gain0
Observed Loss43
Observed Complex0
Frequencyn/a


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