A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv565781



Internal ID16006504
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:100287405..100293628hg38UCSC Ensembl
Innerchr14:100753742..100759965hg19UCSC Ensembl
Innerchr14:99823495..99829718hg18UCSC Ensembl
Cytoband14q32.2
Allele length
AssemblyAllele length
hg386224
hg196224
hg186224
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv833075
Samples
Known GenesSLC25A29
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv565781
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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