A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3638042



Internal ID6678140
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:15877962..15918615hg38UCSC Ensembl
chr16:15971819..16012472hg19UCSC Ensembl
Cytoband16p13.11
Allele length
AssemblyAllele length
hg3840654
hg1940654
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15385660, essv15385682, essv15385679, essv15385672, essv15385658, essv15385661, essv15385671, essv15385657, essv15385656, essv15385669, essv15385650, essv15385681, essv15385673, essv15385652, essv15385676, essv15385677, essv15385666, essv15385653, essv15385649, essv15385654, essv15385664, essv15385680, essv15385665, essv15385651, essv15385655, essv15385663, essv15385670, essv15385662, essv15385667, essv15385675, essv15385659, essv15385674, essv15385668, essv15385678
SamplesHG03351, NA19404, HG03196, HG02952, HG02884, NA20342, NA19461, NA19210, HG00334, HG03548, HG01990, NA19467, HG02455, HG03127, HG03193, HG02577, NA19324, NA19213, NA19360, NA18502, HG03097, HG02511, HG03072, HG02582, NA19235, HG01094, HG03446, NA20287, HG03890, HG02678, NA19095, HG02798, NA19385, HG02095
Known GenesFOPNL
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3638042
Frequency
Sample Size2504
Observed Gain34
Observed Loss0
Observed Complex0
Frequencyn/a


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