A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv565333



Internal ID16352742
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:82931439..82971273hg38UCSC Ensembl
Innerchr14:83397783..83437617hg19UCSC Ensembl
Innerchr14:82467536..82507370hg18UCSC Ensembl
Cytoband14q31.1
Allele length
AssemblyAllele length
hg3839835
hg1939835
hg1839835
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv831077
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv565333
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