A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3620090



Internal ID7006963
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:26119555..26124710hg38UCSC Ensembl
Innerchr9:26119555..26124710hg38UCSC Ensembl
Outerchr9:26119307..26124961hg38UCSC Ensembl
chr9:26119553..26124708hg19UCSC Ensembl
Innerchr9:26119553..26124708hg19UCSC Ensembl
Outerchr9:26119305..26124959hg19UCSC Ensembl
Cytoband9p21.2
Allele length
AssemblyAllele length
hg385156
hg195156
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv13433353, essv13433354
SamplesHG00690, HG02121
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3620090
Frequency
Sample Size2504
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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