A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3621715



Internal ID7008582
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 State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv13618668
SamplesHG00263
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3621715
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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