A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3620366



Internal ID7007237
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:34998944..35002565hg38UCSC Ensembl
Innerchr9:34998961..35002548hg38UCSC Ensembl
Outerchr9:34998927..35002582hg38UCSC Ensembl
chr9:34998941..35002562hg19UCSC Ensembl
Innerchr9:34998958..35002545hg19UCSC Ensembl
Outerchr9:34998924..35002579hg19UCSC Ensembl
Cytoband9p13.3
Allele length
AssemblyAllele length
hg383622
hg193622
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv13459063, essv13459064
SamplesHG00341, HG01271
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3620366
Frequency
Sample Size2504
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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