A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv892e214



Internal ID22756786
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:59386732..59391660hg38UCSC Ensembl
chr3:59372458..59377386hg19UCSC Ensembl
Cytoband3p14.2
Allele length
AssemblyAllele length
hg384929
hg194929
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsesv3596272, esv3596274
SamplesHG02141, HG01600
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)dgv892e214
Frequency
Sample Size2504
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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