A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3620137



Internal ID7007010
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:27740492..27744159hg38UCSC Ensembl
Innerchr9:27740492..27744159hg38UCSC Ensembl
Outerchr9:27740189..27744436hg38UCSC Ensembl
chr9:27740490..27744157hg19UCSC Ensembl
Innerchr9:27740490..27744157hg19UCSC Ensembl
Outerchr9:27740187..27744434hg19UCSC Ensembl
Cytoband9p21.2
Allele length
AssemblyAllele length
hg383668
hg193668
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv13435700
SamplesHG00331
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3620137
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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