A curated catalogue of human genomic structural variation




Variant Details

Variant: essv13560038



Internal ID3561854
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 StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3621095
Supporting Variants
SamplesNA19056
Known GenesSUSD3
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv13560038
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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