A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv449e214



Internal ID22756343
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:41758480..41824304hg38UCSC Ensembl
chr15:42050678..42116502hg19UCSC Ensembl
Cytoband15q15.1
Allele length
AssemblyAllele length
hg3865825
hg1965825
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsesv3636246, esv3636247
SamplesNA20851, HG03886
Known GenesMAPKBP1, MGA
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)dgv449e214
Frequency
Sample Size2504
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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