A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3621759



Internal ID7008625
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:126016054..126020537hg38UCSC Ensembl
Innerchr9:126016066..126020526hg38UCSC Ensembl
Outerchr9:126016043..126020549hg38UCSC Ensembl
chr9:128778333..128782816hg19UCSC Ensembl
Innerchr9:128778345..128782805hg19UCSC Ensembl
Outerchr9:128778322..128782828hg19UCSC Ensembl
Cytoband9q33.3
Allele length
AssemblyAllele length
hg384484
hg194484
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv13619354, essv13619356, essv13619352, essv13619353, essv13619355
SamplesHG01885, NA18504, HG03074, NA19319, HG01058
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3621759
Frequency
Sample Size2504
Observed Gain0
Observed Loss5
Observed Complex0
Frequencyn/a


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