A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4134



Internal ID15548813
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr3:178031129..178043728hg38UCSC Ensembl
Outerchr3:177748917..177761516hg19UCSC Ensembl
Outerchr3:179231611..179244210hg18UCSC Ensembl
Outerchr3:179231619..179244218hg17UCSC Ensembl
Cytoband3q26.32
Allele length
AssemblyAllele length
hg3824056
hg1924056
hg1824056
hg1724056
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv9633
SamplesNA18507
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)nsv4134
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