A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv4768



Internal ID15543191
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr4:97177567..97206783hg38UCSC Ensembl
Outerchr4:98098718..98127934hg19UCSC Ensembl
Outerchr4:98317741..98346957hg18UCSC Ensembl
Outerchr4:98455896..98485112hg17UCSC Ensembl
Cytoband4q22.3
Allele length
AssemblyAllele length
hg385870
hg195870
hg185870
hg175870
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsnsv4435
Supporting Variants
SamplesNA19129
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)nssv4768
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