A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv106e214



Internal ID22756000
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:31965662..31984025hg38UCSC Ensembl
chr10:32254590..32272953hg19UCSC Ensembl
Cytoband10p11.22
Allele length
AssemblyAllele length
hg3818364
hg1918364
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsesv3622819, esv3622820
SamplesNA20321, NA20320, NA19456
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)dgv106e214
Frequency
Sample Size2504
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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