A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3620092



Internal ID7006965
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:26264730..26434172hg38UCSC Ensembl
chr9:26264728..26434170hg19UCSC Ensembl
Cytoband9p21.2
Allele length
AssemblyAllele length
hg38169443
hg19169443
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv13433405, essv13433406
SamplesHG00182, HG01414
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3620092
Frequency
Sample Size2504
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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