A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14247256



Internal ID21301871
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:49896119..50112368hg38UCSC Ensembl
Outerchr11:49891216..50135077hg38UCSC Ensembl
Innerchr11:49917671..50071539hg19UCSC Ensembl
Outerchr11:49912768..50094248hg19UCSC Ensembl
Innerchr11:49874247..50028115hg18UCSC Ensembl
Outerchr11:49869344..50050824hg18UCSC Ensembl
Cytoband11p11.12
Allele length
AssemblyAllele length
hg38243862
hg19181481
hg18181481
Variant TypeCNV duplication
Copy Number4
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3169991
Supporting Variants
SamplesMLY_10
Known GenesOR4C12, OR4C13
MethodSNP array
Analysis
PlatformAffymetrix Genome-wide SNP array 6.0
Comments
ReferenceFu_et_al_2018
Pubmed ID29476164
Accession Number(s)nssv14247256
Frequency
Sample Size93
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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