A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv4864n54



Internal ID22772759
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:2462503..2474820hg38UCSC Ensembl
chr16:2512504..2524821hg19UCSC Ensembl
chr16:2452505..2464822hg18UCSC Ensembl
Cytoband16p13.3
Allele length
AssemblyAllele length
hg3812318
hg1912318
hg1812318
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv571204, nsv571203
Samples
Known GenesC16orf59, MIR6768, NTN3
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv4864n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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