A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv565185



Internal ID16352594
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:74511633..74516366hg38UCSC Ensembl
Innerchr14:74978336..74983069hg19UCSC Ensembl
Innerchr14:74048089..74052822hg18UCSC Ensembl
Cytoband14q24.3
Allele length
AssemblyAllele length
hg384734
hg194734
hg184734
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv829520
Samples
Known GenesLTBP2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv565185
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