A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3620775



Internal ID6660956
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:77482157..77483946hg38UCSC Ensembl
Innerchr9:77482191..77483913hg38UCSC Ensembl
Outerchr9:77482124..77483980hg38UCSC Ensembl
chr9:80097073..80098862hg19UCSC Ensembl
Innerchr9:80097107..80098829hg19UCSC Ensembl
Outerchr9:80097040..80098896hg19UCSC Ensembl
Cytoband9q21.2
Allele length
AssemblyAllele length
hg381790
hg191790
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv13532080, essv13532078, essv13532079
SamplesHG00127, NA20786, NA18988
Known GenesGNA14
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3620775
Frequency
Sample Size2504
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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