A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3616584



Internal ID7003470
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:20919215..20920926hg38UCSC Ensembl
Innerchr8:20919315..20920826hg38UCSC Ensembl
Outerchr8:20919115..20921026hg38UCSC Ensembl
chr8:20776726..20778437hg19UCSC Ensembl
Innerchr8:20776826..20778337hg19UCSC Ensembl
Outerchr8:20776626..20778537hg19UCSC Ensembl
Cytoband8p21.3
Allele length
AssemblyAllele length
hg381712
hg191712
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv13132644, essv13132642, essv13132655, essv13132648, essv13132657, essv13132636, essv13132651, essv13132649, essv13132641, essv13132637, essv13132652, essv13132643, essv13132635, essv13132631, essv13132633, essv13132650, essv13132656, essv13132658, essv13132646, essv13132640, essv13132632, essv13132638, essv13132639, essv13132634, essv13132647, essv13132659, essv13132645, essv13132653, essv13132654
SamplesHG01485, HG00358, NA20514, HG00364, HG03963, NA12058, HG01500, NA11918, HG01080, HG00120, HG03595, HG02502, HG01790, HG00239, NA20525, HG01536, HG00146, HG02256, HG01589, HG01107, HG02660, HG00336, HG00278, NA20544, HG00339, NA11843, NA12154, NA11832, HG00255
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3616584
Frequency
Sample Size2504
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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