A curated catalogue of human genomic structural variation




Variant Details

Variant: essv13559427



Internal ID3193072
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:92230096..92235006hg38UCSC Ensembl
Innerchr9:92230596..92234506hg38UCSC Ensembl
Outerchr9:92229096..92236006hg38UCSC Ensembl
chr9:94992378..94997288hg19UCSC Ensembl
Innerchr9:94992878..94996788hg19UCSC Ensembl
Outerchr9:94991378..94998288hg19UCSC Ensembl
Cytoband9q22.31
Allele length
AssemblyAllele length
hg384911
hg194911
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3621077
Supporting Variants
SamplesHG02807
Known GenesIARS
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv13559427
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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