A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3621080



Internal ID6661261
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:92435546..92479530hg38UCSC Ensembl
Innerchr9:92435546..92479530hg38UCSC Ensembl
Outerchr9:92435046..92480030hg38UCSC Ensembl
chr9:95197828..95241812hg19UCSC Ensembl
Innerchr9:95197828..95241812hg19UCSC Ensembl
Outerchr9:95197328..95242312hg19UCSC Ensembl
Cytoband9q22.31
Allele length
AssemblyAllele length
hg3843985
hg1943985
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv13559430
SamplesNA20507
Known GenesASPN, CENPP
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3621080
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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