A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3621095



Internal ID6661276
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:93064385..93065569hg38UCSC Ensembl
Innerchr9:93064413..93065542hg38UCSC Ensembl
Outerchr9:93064358..93065597hg38UCSC Ensembl
chr9:95826667..95827851hg19UCSC Ensembl
Innerchr9:95826695..95827824hg19UCSC Ensembl
Outerchr9:95826640..95827879hg19UCSC Ensembl
Cytoband9q22.31
Allele length
AssemblyAllele length
hg381185
hg191185
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv13560038
SamplesNA19056
Known GenesSUSD3
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3621095
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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