A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3620894



Internal ID7007764
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:83066037..83068503hg38UCSC Ensembl
Innerchr9:83066061..83068480hg38UCSC Ensembl
Outerchr9:83066014..83068527hg38UCSC Ensembl
chr9:85680952..85683418hg19UCSC Ensembl
Innerchr9:85680976..85683395hg19UCSC Ensembl
Outerchr9:85680929..85683442hg19UCSC Ensembl
Cytoband9q21.32
Allele length
AssemblyAllele length
hg382467
hg192467
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv13538857
SamplesNA19037
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3620894
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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