A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv894e214



Internal ID22756788
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:61077232..61108567hg38UCSC Ensembl
chr3:61062905..61094240hg19UCSC Ensembl
Cytoband3p14.2
Allele length
AssemblyAllele length
hg3831336
hg1931336
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsesv3596328, esv3596329
SamplesNA18621, HG01256
Known GenesFHIT
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)dgv894e214
Frequency
Sample Size2504
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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