A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3620874



Internal ID7007744
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:81806318..81808450hg38UCSC Ensembl
Innerchr9:81806318..81808450hg38UCSC Ensembl
Outerchr9:81806062..81808639hg38UCSC Ensembl
chr9:84421233..84423365hg19UCSC Ensembl
Innerchr9:84421233..84423365hg19UCSC Ensembl
Outerchr9:84420977..84423554hg19UCSC Ensembl
Cytoband9q21.32
Allele length
AssemblyAllele length
hg382133
hg192133
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv13538731, essv13538732, essv13538739, essv13538730, essv13538738, essv13538735, essv13538741, essv13538740, essv13538736, essv13538734, essv13538737, essv13538733, essv13538742
SamplesHG02734, HG01083, HG01110, HG02493, HG03897, NA19917, HG01275, HG03685, HG03740, NA20803, HG03925, HG03698, HG03741
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3620874
Frequency
Sample Size2504
Observed Gain0
Observed Loss13
Observed Complex0
Frequencyn/a


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