A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv7901



Internal ID15189277
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr3:184023744..184056957hg38UCSC Ensembl
Outerchr3:183741532..183774745hg19UCSC Ensembl
Outerchr3:185224226..185257439hg18UCSC Ensembl
Outerchr3:185224234..185257447hg17UCSC Ensembl
Cytoband3q27.1
Allele length
AssemblyAllele length
hg386221
hg196221
hg186221
hg176221
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4145
Supporting Variants
SamplesNA12156
Known GenesHTR3C, HTR3D
MethodSequencing
AnalysisEnd-sequence pairs were mapped to the human genome assembly (hg17) using a previously described algorithm (Tuzun et al 2005)
PlatformCapillary
Comments
ReferenceKidd_et_al_2008
Pubmed ID18451855
Accession Number(s)nssv7901
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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