A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3984389



Internal ID19208779
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr1:434937..452937hg38UCSC Ensembl
Outerchr1:366400..384400hg19UCSC Ensembl
Cytoband1p36.33
Allele length
AssemblyAllele length
hg3818001
hg1918001
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1126162
Supporting Variants
SamplesKWS1
Known GenesOR4F16, OR4F29, OR4F3
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nssv3984389
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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