A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv4916n54



Internal ID18997092
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:14690312..14742768hg38UCSC Ensembl
chr16:14784169..14836625hg19UCSC Ensembl
chr16:14691670..14744126hg18UCSC Ensembl
Cytoband16p13.11
Allele length
AssemblyAllele length
hg3852457
hg1952457
hg1852457
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv571508, nsv571515, nsv571509
Samples
Known GenesNPIPA2, NPIPA3, PLA2G10
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv4916n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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