A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv1279e214



Internal ID22757173
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:34049763..34077048hg38UCSC Ensembl
chr7:34089375..34116660hg19UCSC Ensembl
Cytoband7p14.3
Allele length
AssemblyAllele length
hg3827286
hg1927286
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsesv3612787, esv3612789
SamplesNA12273, HG00148
Known GenesBMPER
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)dgv1279e214
Frequency
Sample Size2504
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer