A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv473e214



Internal ID22756367
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:1356674..1364974hg38UCSC Ensembl
chr16:1406675..1414975hg19UCSC Ensembl
Cytoband16p13.3
Allele length
AssemblyAllele length
hg388301
hg198301
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsesv3637614, esv3637615
SamplesHG03517, HG02922, HG00629, HG00266, HG03511
Known GenesGNPTG, UNKL
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)dgv473e214
Frequency
Sample Size2504
Observed Gain0
Observed Loss5
Observed Complex0
Frequencyn/a


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