A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3621084



Internal ID6661265
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:92580135..92582715hg38UCSC Ensembl
Innerchr9:92580135..92582715hg38UCSC Ensembl
Outerchr9:92579938..92582959hg38UCSC Ensembl
chr9:95342417..95344997hg19UCSC Ensembl
Innerchr9:95342417..95344997hg19UCSC Ensembl
Outerchr9:95342220..95345241hg19UCSC Ensembl
Cytoband9q22.31
Allele length
AssemblyAllele length
hg382581
hg192581
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv13559437
SamplesNA19900
Known GenesCENPP
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3621084
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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