A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv563852



Internal ID16004575
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:21737165..21875978hg38UCSC Ensembl
Innerchr14:22205447..22344160hg19UCSC Ensembl
Innerchr14:21275287..21414000hg18UCSC Ensembl
Cytoband14q11.2
Allele length
AssemblyAllele length
hg38138814
hg19138714
hg18138714
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv823020
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv563852
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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