A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv1315e214



Internal ID22757209
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:104579982..104609634hg38UCSC Ensembl
chr7:104220429..104250081hg19UCSC Ensembl
Cytoband7q22.2
Allele length
AssemblyAllele length
hg3829653
hg1929653
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsesv3614398, esv3614397
SamplesHG03986, NA19036, NA19445, HG03755, NA19429
Known GenesLHFPL3
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)dgv1315e214
Frequency
Sample Size2504
Observed Gain0
Observed Loss5
Observed Complex0
Frequencyn/a


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