A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv958751



Internal ID17307624
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr14:79187564..79187690hg38UCSC Ensembl
Outerchr14:79653907..79654033hg19UCSC Ensembl
Cytoband14q31.1
Allele length
AssemblyAllele length
hg38127
hg19127
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3005425
SamplesBILGI_BIOE
Known GenesNRXN3
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceDogan_et_al_2014
Pubmed ID24416366
Accession Number(s)nsv958751
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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