A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5865



Internal ID15204031
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr7:99656798..99690110hg38UCSC Ensembl
Outerchr7:99254421..99287733hg19UCSC Ensembl
Outerchr7:99092357..99125669hg18UCSC Ensembl
Outerchr7:98899072..98932384hg17UCSC Ensembl
Cytoband7q22.1
Allele length
AssemblyAllele length
hg386720
hg196720
hg186720
hg176720
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2676
SamplesNA18555
Known GenesCYP3A5, CYP3A7-CYP3AP1
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)nsv5865
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