A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv2426



Internal ID15540706
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr3:155362287..155392861hg38UCSC Ensembl
Outerchr3:155080076..155110650hg19UCSC Ensembl
Outerchr3:156562770..156593344hg18UCSC Ensembl
Outerchr3:156562778..156593352hg17UCSC Ensembl
Cytoband3q25.31
Allele length
AssemblyAllele length
hg389456
hg199456
hg189456
hg179456
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4075
Supporting Variants
SamplesNA18555
Known Genes
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)nssv2426
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