A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv1334e214



Internal ID22757228
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:148897466..148924236hg38UCSC Ensembl
chr7:148594558..148621328hg19UCSC Ensembl
Cytoband7q36.1
Allele length
AssemblyAllele length
hg3826771
hg1926771
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsesv3615419, esv3615418
SamplesNA19011, HG01516
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)dgv1334e214
Frequency
Sample Size2504
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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