A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv102e214



Internal ID22755996
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:20492763..20534910hg38UCSC Ensembl
chr10:20781692..20823839hg19UCSC Ensembl
Cytoband10p12.31
Allele length
AssemblyAllele length
hg3842148
hg1942148
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsesv3622556, esv3622557
SamplesNA11829, HG01374, HG00246, NA20826
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)dgv102e214
Frequency
Sample Size2504
Observed Gain4
Observed Loss0
Observed Complex0
Frequencyn/a


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