A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3136



Internal ID15540839
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr4:111689743..111723920hg38UCSC Ensembl
Outerchr4:112610899..112645076hg19UCSC Ensembl
Outerchr4:112830348..112864525hg18UCSC Ensembl
Outerchr4:112968503..113002680hg17UCSC Ensembl
Cytoband4q25
Allele length
AssemblyAllele length
hg385847
hg195847
hg185847
hg175847
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4468
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)nssv3136
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