A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv2618



Internal ID15193809
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr6:143603100..143634776hg38UCSC Ensembl
Outerchr6:143924237..143955913hg19UCSC Ensembl
Outerchr6:143965930..143997606hg18UCSC Ensembl
Outerchr6:143965930..143997606hg17UCSC Ensembl
Cytoband6q24.2
Allele length
AssemblyAllele length
hg388344
hg198344
hg188344
hg178344
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5512
Supporting Variants
SamplesNA18555
Known GenesPHACTR2
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)nssv2618
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