A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3614338



Internal ID7001232
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:101737597..101740818hg38UCSC Ensembl
Innerchr7:101737597..101740818hg38UCSC Ensembl
Outerchr7:101737097..101741318hg38UCSC Ensembl
chr7:101380877..101384098hg19UCSC Ensembl
Innerchr7:101380877..101384098hg19UCSC Ensembl
Outerchr7:101380377..101384598hg19UCSC Ensembl
Cytoband7q22.1
Allele length
AssemblyAllele length
hg383222
hg193222
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv12910908, essv12910905, essv12910900, essv12910887, essv12910875, essv12910899, essv12910907, essv12910894, essv12910879, essv12910888, essv12910891, essv12910898, essv12910901, essv12910902, essv12910874, essv12910878, essv12910903, essv12910884, essv12910895, essv12910877, essv12910906, essv12910892, essv12910880, essv12910881, essv12910889, essv12910897, essv12910890, essv12910883, essv12910885, essv12910876, essv12910904, essv12910886, essv12910893, essv12910882, essv12910896
SamplesNA19700, NA19909, HG03175, HG03247, HG02804, HG02769, HG03464, NA18489, HG01488, HG02541, HG02325, NA19198, NA20287, HG02315, NA19917, HG01308, HG02427, NA20127, HG02477, NA19184, HG02511, NA19327, HG02497, HG02537, NA19042, NA19031, NA19095, NA19395, NA19149, HG02983, NA19472, NA19093, NA18873, HG02947, NA19312
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3614338
Frequency
Sample Size2504
Observed Gain0
Observed Loss35
Observed Complex0
Frequencyn/a


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