A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv564700



Internal ID16352109
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:44647775..44765043hg38UCSC Ensembl
Innerchr14:45116978..45234246hg19UCSC Ensembl
Innerchr14:44186728..44303996hg18UCSC Ensembl
Cytoband14q21.2
Allele length
AssemblyAllele length
hg38117269
hg19117269
hg18117269
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv827613
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv564700
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