A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv1436e214



Internal ID22757330
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:7288275..7373570hg38UCSC Ensembl
chr9:7288275..7373570hg19UCSC Ensembl
Cytoband9p24.1
Allele length
AssemblyAllele length
hg3885296
hg1985296
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsesv3619459, esv3619461
SamplesNA18608
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)dgv1436e214
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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