A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3620977



Internal ID7007847
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:87259649..87264669hg38UCSC Ensembl
Innerchr9:87259649..87264669hg38UCSC Ensembl
Outerchr9:87259416..87264873hg38UCSC Ensembl
chr9:89874564..89879584hg19UCSC Ensembl
Innerchr9:89874564..89879584hg19UCSC Ensembl
Outerchr9:89874331..89879788hg19UCSC Ensembl
Cytoband9q21.33
Allele length
AssemblyAllele length
hg385021
hg195021
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv13547000, essv13547002, essv13547003, essv13547001
SamplesNA19723, HG02143, HG02588, HG02721
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3620977
Frequency
Sample Size2504
Observed Gain0
Observed Loss4
Observed Complex0
Frequencyn/a


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