A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3619890



Internal ID6660076
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:19111295..19128047hg38UCSC Ensembl
Innerchr9:19111295..19128047hg38UCSC Ensembl
Outerchr9:19110795..19128547hg38UCSC Ensembl
chr9:19111293..19128045hg19UCSC Ensembl
Innerchr9:19111293..19128045hg19UCSC Ensembl
Outerchr9:19110793..19128545hg19UCSC Ensembl
Cytoband9p22.1
Allele length
AssemblyAllele length
hg3816753
hg1916753
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv13415201, essv13415202
SamplesHG00737, HG01162
Known GenesPLIN2
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3619890
Frequency
Sample Size2504
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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