A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv1465e214



Internal ID22757359
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:28529033..28735701hg38UCSC Ensembl
chr9:28529031..28735699hg19UCSC Ensembl
Cytoband9p21.1
Allele length
AssemblyAllele length
hg38206669
hg19206669
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsesv3620168, esv3620170
SamplesHG00177, NA07357, HG00243, NA20759, HG00106, NA19921, HG04195, HG04017, NA18865
Known GenesLINGO2
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)dgv1465e214
Frequency
Sample Size2504
Observed Gain0
Observed Loss9
Observed Complex0
Frequencyn/a


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