A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3621013



Internal ID7007883
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:88830313..88833218hg38UCSC Ensembl
Innerchr9:88830320..88833212hg38UCSC Ensembl
Outerchr9:88830307..88833225hg38UCSC Ensembl
chr9:91445228..91448133hg19UCSC Ensembl
Innerchr9:91445235..91448127hg19UCSC Ensembl
Outerchr9:91445222..91448140hg19UCSC Ensembl
Cytoband9q22.1
Allele length
AssemblyAllele length
hg382906
hg192906
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv13549491
SamplesHG01707
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3621013
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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