A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv565205



Internal ID16352614
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:75553412..75579019hg38UCSC Ensembl
Innerchr14:76019755..76045362hg19UCSC Ensembl
Innerchr14:75089508..75115115hg18UCSC Ensembl
Cytoband14q24.3
Allele length
AssemblyAllele length
hg3825608
hg1925608
hg1825608
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1148958
SamplesHGDP01169
Known GenesFLVCR2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv565205
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