A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3619019



Internal ID7005900
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:139498172..139600722hg38UCSC Ensembl
Innerchr8:139498313..139600581hg38UCSC Ensembl
Outerchr8:139498031..139600863hg38UCSC Ensembl
chr8:140510415..140612965hg19UCSC Ensembl
Innerchr8:140510556..140612824hg19UCSC Ensembl
Outerchr8:140510274..140613106hg19UCSC Ensembl
Cytoband8q24.3
Allele length
AssemblyAllele length
hg38102551
hg19102551
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv13351521, essv13351535, essv13351516, essv13351534, essv13351522, essv13351529, essv13351520, essv13351530, essv13351533, essv13351517, essv13351537, essv13351542, essv13351544, essv13351519, essv13351541, essv13351513, essv13351532, essv13351515, essv13351527, essv13351523, essv13351528, essv13351524, essv13351539, essv13351512, essv13351525, essv13351531, essv13351543, essv13351514, essv13351526, essv13351536, essv13351538, essv13351518, essv13351540
SamplesNA12414, HG00103, NA12058, NA12399, HG00327, HG01500, HG00138, NA12283, HG00369, NA12282, HG01067, HG01527, HG01284, HG01771, NA11831, HG01784, HG00380, HG01684, NA12718, HG00239, HG01390, NA12144, NA19017, HG03778, NA12716, HG00375, HG02232, HG00237, HG01765, HG00112, HG00343, HG01479, HG01437
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3619019
Frequency
Sample Size2504
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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