A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3621077



Internal ID7007947
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 State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv13559427
SamplesHG02807
Known GenesIARS
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3621077
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer