A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3638018



Internal ID6678116
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:15005446..15029641hg38UCSC Ensembl
chr16:15099303..15123498hg19UCSC Ensembl
Cytoband16p13.11
Allele length
AssemblyAllele length
hg3824196
hg1924196
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv482e214
Supporting Variantsessv15385497, essv15385496, essv15385480, essv15385486, essv15385483, essv15385485, essv15385492, essv15385494, essv15385489, essv15385498, essv15385487, essv15385491, essv15385481, essv15385493, essv15385495, essv15385490, essv15385482, essv15385484, essv15385488
SamplesNA21099, HG00766, HG03518, HG02888, HG03199, NA18944, HG01501, NA21098, HG03294, HG02219, NA21142, HG01204, NA21143, NA19256, HG01375, NA20786, HG01468, HG03072, HG04161
Known GenesPDXDC1
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3638018
Frequency
Sample Size2504
Observed Gain19
Observed Loss0
Observed Complex0
Frequencyn/a


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