A curated catalogue of human genomic structural variation




Variant Details

Variant: essv13618668



Internal ID603675
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:124174437..124176012hg38UCSC Ensembl
Innerchr9:124174453..124175996hg38UCSC Ensembl
Outerchr9:124174421..124176028hg38UCSC Ensembl
chr9:126936716..126938291hg19UCSC Ensembl
Innerchr9:126936732..126938275hg19UCSC Ensembl
Outerchr9:126936700..126938307hg19UCSC Ensembl
Cytoband9q33.3
Allele length
AssemblyAllele length
hg381576
hg191576
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3621715
Supporting Variants
SamplesHG00263
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv13618668
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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