A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv901584



Internal ID6263511
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:31365884..31405153hg19UCSC Ensembl
Outerchr14:31358377..31409010hg19UCSC Ensembl
Innerchr14:30435635..30474904hg18UCSC Ensembl
Outerchr14:30428128..30478761hg18UCSC Ensembl
Cytoband14q12
Allele length
AssemblyAllele length
hg19n/a
hg18n/a
Variant TypeCNV Loss
Copy Number
Allele State
Allele Origin
Probe Count
Merged StatusS
Merged Variants
Supporting Variantsnssv1570015
SamplesIS31765
Known GenesCOCH, LOC100506071, STRN3
Method
Analysis
PlatformIllumina HumanHap 610 Quad + Illumina HumanHap 1MduoV3
Comments
ReferenceXu_et_al_2011
Pubmed ID21882294
Accession Number(s)nsv901584
Frequency
Sample Size6533
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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