A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3621048



Internal ID7007918
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:90655588..91365881hg38UCSC Ensembl
Innerchr9:90655738..91365731hg38UCSC Ensembl
Outerchr9:90655438..91366031hg38UCSC Ensembl
chr9:93417870..94128163hg19UCSC Ensembl
Innerchr9:93418020..94128013hg19UCSC Ensembl
Outerchr9:93417720..94128313hg19UCSC Ensembl
Cytoband9q22.2
Allele length
AssemblyAllele length
hg38710294
hg19710294
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv13555487
SamplesHG01602
Known GenesAUH, LOC100129316, SYK
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3621048
Frequency
Sample Size2504
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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