A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv1269e214



Internal ID22757163
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:14069653..14140649hg38UCSC Ensembl
chr7:14109278..14180274hg19UCSC Ensembl
Cytoband7p21.2
Allele length
AssemblyAllele length
hg3870997
hg1970997
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsesv3612307, esv3612309
SamplesNA20832
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)dgv1269e214
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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