A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv448e214



Internal ID22756342
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:34238802..34242962hg38UCSC Ensembl
chr15:34531003..34535163hg19UCSC Ensembl
Cytoband15q14
Allele length
AssemblyAllele length
hg384161
hg194161
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsesv3636105, esv3636107
SamplesNA19700, HG03052
Known GenesSLC12A6
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)dgv448e214
Frequency
Sample Size2504
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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